A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy

Overview of attention for article published in Frontiers in Genetics, October 2021

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New Research: A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy: Merosine deficient congenital muscular dystrophy is one of the most common forms of congenital muscular dystrophy. This disease is… https://t.co

29 Oct 2021

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