https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2023.1191068/full
Frontiers | Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2...
Mutations of LAMA2 gene are associated with congenital muscular dystrophy (CMD). The LAMA2-related CMD mainly consists of two diseases, merosin deficient con...
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https://pubmed.ncbi.nlm.nih.gov/35924034/?dopt=Abstract
A rare case of arrhythmogenic right ventricular cardiomyopathy associated with LAMA2 mutation: A...
rare case