Review
A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.
J. Appl. Genet. 2019 May 1; 60 (2): 151-162.
Article
A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability.
Brain Dev. 2018 Jan 1; 40 (1): 58-64.
Article
Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family.
Pak J Med Sci. 2019 Jan 1; 35 (3): 764-770.