MeSH Browser

MeSH Supplementary: DYSF protein, human
Unique ID: C114839
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C114839
Entry Term(s): dysferlin protein, human; dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) protein, human; dysferlin-v1 protein, human
Previous Indexing: *MEMBRANE PROTEINS (1998-2017); *MUSCLE PROTEINS (1998-2017)
Heading Mapped to: *Dysferlin
Frequency: 378
Note: dysferlin is a skeletal muscle gene mutated in Miyoshi myopathy & limb girdle muscular dystrophy, RefSeq NM_003494
Source: Nat Genet 1998 Sep;20(1):31-6
Indexing Information: Muscular Dystrophies
Date of Entry: 1998/10/19
Revision Date: 2017/09/22

DYSF protein, human MeSH Supplementary Concept Data 2024