Mahdieh Rahimoghli on Muck Rack

Mahdieh Rahimoghli

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Articles

Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy - Journal of Human Genetics

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By Mahsa Mohammadi, Aida Ghasemi, Ali Asghar Okhovat, Afagh Alavi, Mahdieh Rahimoghli
| Nature Verified
Abstract The LAMA2 gene encodes the alpha-2 chain of laminin-2, a key component of the basement membrane that maintains muscle fiber stability and integrity. Mutations in this gene are linked with LAMA2-related muscular dystrophies, which includes congenital muscular dystrophy type 1 A (MDC1A) and limb-girdle muscular dystrophy autosomal recessive 23 (LGMDR23).
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