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ArticleJournal of human genetics2024

A novel heterozygous TMEM63A variant in a familial case with early onset nystagmus, severe hypomyelination, and a favorable adult prognosis.

Shota Yoneno et al.PubMed ↗Publisher ↗

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4 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 38951194