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Genetic analysis in three Egyptian patients with Griscelli syndrome Type 1 reveals new nonsense mutations in MYO5A.

Clinical and experimental dermatology - 1 Aug 2020

Abd Elmaksoud M S, Gomaa N S, Azouz H G, On C N V, Ho C T, Omar T E, McGrath J A, Onoufriadis A

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32275080
DOI: 10.1111/ced.14220

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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