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Matches in Nanopublications for { ?s ?p "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP916498.RAcZ7TXD9VjpRRr_uWp2zuKGdAmJZaPeg8wlNMLkCbf5o130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916498.RAcZ7TXD9VjpRRr_uWp2zuKGdAmJZaPeg8wlNMLkCbf5o130_provenance.
• NP323016.RADGF6CKfTz-1xjK8yP82B-gXpHXhbDl3a4mmCxr0EBpY130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323016.RADGF6CKfTz-1xjK8yP82B-gXpHXhbDl3a4mmCxr0EBpY130_provenance.
• NP738555.RA6j_vbHNvsLeIerrq13XTYHTDBvy7alyUBuBeFIAGtGI130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738555.RA6j_vbHNvsLeIerrq13XTYHTDBvy7alyUBuBeFIAGtGI130_provenance.
• NP436333.RA8nPAk6L2RZeBohjGEgMhFFXlYgUx0e3-0PToyu3M6PM130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436333.RA8nPAk6L2RZeBohjGEgMhFFXlYgUx0e3-0PToyu3M6PM130_provenance.
• NP630785.RAysCyWotN7QQ8uuCCkzwGxmJiLOaL4lO6CRfCfg5-ePI130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630785.RAysCyWotN7QQ8uuCCkzwGxmJiLOaL4lO6CRfCfg5-ePI130_provenance.
• NP630787.RA0XJVChLNUEfrkvzi0Z73vVN_r-Itp6iW7fy1vY-yCgU130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630787.RA0XJVChLNUEfrkvzi0Z73vVN_r-Itp6iW7fy1vY-yCgU130_provenance.
• NP324407.RAgwLHcaar33oSwN-gFHu4r7zvK3CPPXqJ4o17lWsIqSo130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324407.RAgwLHcaar33oSwN-gFHu4r7zvK3CPPXqJ4o17lWsIqSo130_provenance.
• NP630783.RAOhEaTAcQKJu2Lx3JPyGeoti32uBxRS6o93mDOSwkmzE130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630783.RAOhEaTAcQKJu2Lx3JPyGeoti32uBxRS6o93mDOSwkmzE130_provenance.
• NP822019.RAqhSpKtRNcyluciHFNPW4OnIpXDi38nYpEAih4gdOlwI130_assertion description "[Neurological diagnostic workup in these patients revealed weakness, wasting, reduced/exaggerated tendon reflexes, abnormal nerve conduction and electromyography, muscle biopsy with ragged red muscle fibers, reduced COX staining, decreased complex I respiratory chain activity, abnormally structured mitochondria, or mitochondrial DNA (mtDNA) mutations, such as G5650A in the tRNAAla gene, or various other mtDNA substitutions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822019.RAqhSpKtRNcyluciHFNPW4OnIpXDi38nYpEAih4gdOlwI130_provenance.