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. (Q41752195)
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scientific article published on May 2015
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English | 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. |
scientific article published on May 2015 |
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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. (English)
1 reference
Saleem Ahmed
Nuha Alrayes
Hussein Sheikh Ali Mohamoud
Mona Mohammad Almramhi
Wasim Anshasi
Naushad Ali Basheer Ahmed
Jamal Nasir
Jumana Yousuf Al-Aama