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

Research output: Contribution to journalArticle

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

Original languageEnglish
JournalClinical and Experimental Dermatology
Publication statusAccepted/In press - 1 Jan 2020

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