Varaico: Literature-Extracted Genetic Variants

Gene:SEMA3D
Variant:p.E198K
Back to variants list

SEMA3D

NM_001384900.1:p.E198K

Associated Papers

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.

Luzón-Toro B et al.

Scientific Reports, 2015

Mutational spectrum of semaphorin 3A and semaphorin 3D genes in Spanish Hirschsprung patients.

Luzón-Toro B et al.

Plos One, 2013

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."