WDR62 missense mutation in a consanguineous family with primary microcephaly
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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2. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations;Bilguvar;Nature,2010
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1. Autosomal Recessive Primary Microcephaly: Not Just a Small Brain;Frontiers in Cell and Developmental Biology;2022-01-17
2. Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene;Genes;2021-04-19
3. Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry;PLOS Biology;2020-08-06
4. Two Novel Mutations (c.883-4_890del and c.1684C>G) of WDR62 Gene Associated With Autosomal Recessive Primary Microcephaly: A Case Report;Frontiers in Pediatrics;2019-11-07
5. A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature;Journal of Applied Genetics;2019-02-01
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