Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.
In conclusion, the majority of Serbian LGMD2A patients have the same mutation and similar phenotype.
PMID: 31788660 [PubMed - in process]
Source: Acta Myologica - Category: Neurology Tags: Acta Myol Source Type: research
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