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F Al-Moayyad

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Shen J, Eyaid W, Mochida G, Al-Moayyad F, Bodell A, Woods C, et al.
J Med Genet . 2005 Sep; 42(9):725-9. PMID: 16141009
Background: Human autosomal recessive primary microcephaly (MCPH) is a heterogeneous disorder with at least six genetic loci (MCPH1-6), with MCPH5, caused by ASPM mutation, being the most common. Despite the...