Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients

Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients

BackgroundLAMA2-related limb girdle muscular dystrophy (LGMD R23) is rare. The detailed clinical phenotypes and genetic information associated with LGMD R23 are unknown.MethodsWe conducted a retrospective cross-sectional and longitudinal study on 19 LGMD R23 patients.ResultsNormal early motor develo...

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Bibliographic Details
Main Authors: Xiuli Huang, Dandan Tan, Zaiqiang Zhang, Lin Ge, Jieyu Liu, Juan Ding, Haipo Yang, Cuijie Wei, Xingzhi Chang, Yun Yuan, Chuanzhu Yan, Hui Xiong
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-05-01
Series:Frontiers in Neurology
Subjects:
LAMA2-related limb girdle muscular dystrophy
LGMD R23
phenotype
genotype
genotype-phenotype correlations
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2023.1158094/full

Internet

https://www.frontiersin.org/articles/10.3389/fneur.2023.1158094/full

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