Varaico: Literature-Extracted Genetic Variants

Gene:CNTLN
Variant:p.A805S
Back to variants list

CNTLN

NM_017738.4:p.A805S

Associated Papers

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

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."