Associated Papers
Functional analysis of a novel intronic variant of MCPH1 with autosomal recessive primary microcephaly.
Luo S et al.
Heliyon, 2024
MCPH1: A Novel Case Report and a Review of the Literature.
Caraffi SG et al.
Genes, 2022
35456440 (PubMed )
Supplement: genes-13-00634-s001.zip › Table_S1-MCPH1_Case_Report_v_Literature.xlsx › Table_S1
Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family.
Naseer MI et al.
Neurosciences (riyadh, Saudi Arabia), 2018
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