Novel five nucleotide deletion in dysferlin leads to autosomal recessive limb‐girdle muscular dystrophy

Novel five nucleotide deletion in dysferlin leads to autosomal recessive limb‐girdle muscular dystrophy

Abstract Muscular dystrophy (MD) is a genetic disorder that causes progressive muscle weakness and degeneration. Limb‐girdle muscular dystrophy (LGMD) is a type of MD that mainly causes muscle atrophy within the shoulder and pelvic girdles. LGMD is classified into autosomal dominant (LGMD‐D) and aut...

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Bibliographic Details
Main Authors: Yen‐Lin Chen, Wen‐Bin Wu, Pei Wang, Ping‐Keung Yip, Yi‐No Wu, Ying‐Hung Lin, Wei‐Ning Lin
Format: Article
Language:English
Published: Wiley 2023-12-01
Series:Physiological Reports
Subjects:
dysferlin
heterozygous mutation
limb‐girdle muscular dystrophy
Online Access:https://doi.org/10.14814/phy2.15887

Internet

https://doi.org/10.14814/phy2.15887

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