1.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, S, Jelani, M,
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Ahmed, S, Jelani, M, Alrayes, N, Mohamoud, HSA, Almramhi, MM, Anshasi, W, Ahmed, NAB, Wang, J, Nasir, J, Al-Aama, JY
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JOURNAL OF THE NEUROLOGICAL SCIENCES[0022-510X],
Published 2015,
Volume 353,
Issue 1-2,
Pages 149-154
收錄情况:
WOS
WOS核心合集引用: 31
2022影響因子:
4.4
发表年影響因子:
2.126