Varaico: Literature-Extracted Genetic Variants

Gene:WNT10A
Variant:p.N106K
Back to variants list

WNT10A

NM_025216.3:p.N106K

Associated Papers

Analyses of oligodontia phenotypes and genetic etiologies.

Zhou M et al.

International Journal of Oral Science, 2021

Schöpf-Schulz-Passarge syndrome associated with two new missense mutations in WNT10A.

Pauly KJ et al.

Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : Jddg, 2018

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."