Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients
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DOI: 10.3389/fneur.2023.1158094
Abstract: Background LAMA2-related limb girdle muscular dystrophy (LGMD R23) is rare. The detailed clinical phenotypes and genetic information associated with LGMD R23 are unknown. Methods We conducted a retrospective cross-sectional and longitudinal study on 19 LGMD… read more here.
Keywords: lama2 related; related limb; limb girdle; muscular dystrophy ... See more keywords