Associated Papers
Neurological outcome in WDR62 primary microcephaly.
Ruaud L et al.
Developmental Medicine and Child Neurology, 2022
Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene.
Slezak R et al.
Genes, 2021
33921653 (PubMed )
Supplement: genes-12-00594-s001.zip › genes-1145756-supplementary.pdf
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.
Rasool S et al.
Molecular Genetics & Genomic Medicine, 2020
A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.
Zombor M et al.
Journal of Applied Genetics, 2019
Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family.
Naseer MI et al.
Pakistan Journal of Medical Sciences, 2019
The Role of WD40-Repeat Protein 62 (MCPH2) in Brain Growth: Diverse Molecular and Cellular Mechanisms Required for Cortical Development.
Shohayeb B et al.
Molecular Neurobiology, 2018
A novel single base pair duplication in WDR62 causes primary microcephaly.
Rupp V et al.
Bmc Medical Genetics, 2014
The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome.
McDonell LM et al.
Bmc Neurology, 2014
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation.
Farag HG et al.
Orphanet Journal of Rare Diseases, 2013
A novel WDR62 mutation causes primary microcephaly in a Pakistani family.
Memon MM et al.
Molecular Biology Reports, 2013
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.
Naseer MI et al.
Annals of Saudi Medicine, 0
Select a paper to view details