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
Ahmed, Saleem, Jelani, Musharraf, Alrayes, Nuha, Mohamoud, Hussein Sheikh Ali, Almramhi, Mona Mohammad, Anshasi, Wasim, Ahmed, Naushad Ali Basheer, Wang, Jun, Nasir, Jamal, Al-Aama, Jumana Yousuf
Published in Journal of the neurological sciences (15.06.2015)
Published in Journal of the neurological sciences (15.06.2015)
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