Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3

Saleem Ahmed(King Abdulaziz University), Musharraf Jelani(St George's, University of London), Nuha Alrayes(St George's, University of London), Hussein Sheikh Ali Mohamoud(St George's, University of London), Mona Mohammad Almramhi(King Abdulaziz University), Wasim Anshasi(King Abdulaziz University), Naushad Ahmed(King Abdulaziz Hospital), Jun Wang(BGI Group (China)), Jamal Nasir(St George's, University of London), Jumana Y. Al‐Aama(King Abdulaziz University)
Journal of the Neurological Sciences
May 3, 2015
Cited by 44

Abstract


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