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ArticleActa neurologica Belgica2021

Identification of a novel missense c.386G > A variant in a boy with the POMGNT1-related muscular dystrophy-dystroglycanopathy.

Pouria Mohammadi et al.PubMed ↗Publisher ↗

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7 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 33175337