Matches in Nanopublications for { ?s ?p "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP378647.RARxy-25wRhAwq5zF7T0IZ1oyDGQFfw8N9VUkPry9g068130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378647.RARxy-25wRhAwq5zF7T0IZ1oyDGQFfw8N9VUkPry9g068130_provenance.
- NP422247.RAkRDPCcRTwXPyP2ghRV3_6XFH9_r6otenhYRWjXafPAg130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422247.RAkRDPCcRTwXPyP2ghRV3_6XFH9_r6otenhYRWjXafPAg130_provenance.
- NP322363.RALBFSVt9UheA5i88Tp2QvS_hBRODhiF0O9ydqdZdi0w8130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322363.RALBFSVt9UheA5i88Tp2QvS_hBRODhiF0O9ydqdZdi0w8130_provenance.
- NP917689.RALXT7mWPZ2HD9f7N76XczDllDN0k9jOJkdrPewNNHIYc130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917689.RALXT7mWPZ2HD9f7N76XczDllDN0k9jOJkdrPewNNHIYc130_provenance.
- NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486909.RATgopwc0OD-tNI6IV3Qd4_slkmWHfMjQ-eojK_r3ZsHE130_provenance.
- NP486906.RAM3DiB2hGP25f-cbks-JkjSEXhGk71AcUMXS07BFivAk130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486906.RAM3DiB2hGP25f-cbks-JkjSEXhGk71AcUMXS07BFivAk130_provenance.
- NP1011886.RAPvyNeDvDzNp0ylqAKIHJrW0pfvuSlIGjMTd-OII8YkU130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011886.RAPvyNeDvDzNp0ylqAKIHJrW0pfvuSlIGjMTd-OII8YkU130_provenance.
- NP1011885.RAlLZjgACwt2oYkQy3gJVT2_BcTjDJhmmFd1ilZphaTqI130_assertion description "[Mutations in immunoglobulin µ-binding protein 2 (Ighmbp2) cause distal spinal muscular atrophy type 1 (DSMA1), an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011885.RAlLZjgACwt2oYkQy3gJVT2_BcTjDJhmmFd1ilZphaTqI130_provenance.