Varaico: Literature-Extracted Genetic Variants

Gene:LAMA3
Variant:p.N1131insFs
Back to variants list

LAMA3

NM_000227.6:p.N1131insFs

Associated Papers

Carriers with functional null mutations in LAMA3 have localized enamel abnormalities due to haploinsufficiency.

Gostyńska KB et al.

European Journal of Human Genetics : Ejhg, 2016

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."