Matches in Nanopublications for { ?s ?p "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- NP450921.RANj4ABiG0H6sN1F9pqFwX40BCChZLQWZDWffCX1DTTeA130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450921.RANj4ABiG0H6sN1F9pqFwX40BCChZLQWZDWffCX1DTTeA130_provenance.
- NP398674.RAH42gBZlWCd2mDBuKDiMIk18tIhf1wqhqRxHRP0zrzFU130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398674.RAH42gBZlWCd2mDBuKDiMIk18tIhf1wqhqRxHRP0zrzFU130_provenance.
- NP630716.RAB1zYlc4bLK2FvyfUpIJABUmUJJmBBHS-CNEb3w6ScBs130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630716.RAB1zYlc4bLK2FvyfUpIJABUmUJJmBBHS-CNEb3w6ScBs130_provenance.
- NP777256.RA5ImJr1X_PP8n7d0GK-Uz5d3wSMyibXgX0Cr2zeDECBU130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777256.RA5ImJr1X_PP8n7d0GK-Uz5d3wSMyibXgX0Cr2zeDECBU130_provenance.
- NP777258.RA0-Yil2DzYcxejT8MMNg-uaS_lA0z_2thCEUzkmHK0ts130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777258.RA0-Yil2DzYcxejT8MMNg-uaS_lA0z_2thCEUzkmHK0ts130_provenance.
- assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP777257.RAb83LWaeg-tcgkp_n6B8Et-wXcriqn0NMa0uKrHLwfwI130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777257.RAb83LWaeg-tcgkp_n6B8Et-wXcriqn0NMa0uKrHLwfwI130_provenance.
- NP630736.RAOdQ3Dxfke_CorgS5diSbOX25UrC5Qvnw60CIQjUULUE130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630736.RAOdQ3Dxfke_CorgS5diSbOX25UrC5Qvnw60CIQjUULUE130_provenance.
- NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630750.RAsYYuA_-uX6ZdfdkCmF2pe4tKAIKv_0EcO48xwWY5xlE130_provenance.