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Article

DYNC2H1 variants cause Leber congenital amaurosis without syndromic features.

Clinical genetics - 1 Jul 2021

Lee Junwon, Lee Hyunjoo, Lee Young-Mock, Kuht Helen J, Thomas Mervyn G, Kim Sang Jin, Lee Seung-Tae, Han Jinu

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Share to Amino Acid Sequence
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 33755199
DOI: 10.1111/cge.13958

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