Modifier variant of METTL13 suppresses human GAB1–associated profound deafness
Author:
Funder
National Institute on Deafness and Other Communication Disorders
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/97350/files/pdf
Reference64 articles.
1. Functional variants in the lipoprotein lipase gene and risk of cardiovascular disease
2. The role of gene-environment interaction in the aetiology of human cancer: examples from cancers of the large bowel, lung and breast
3. Early-onset Alzheimer’s disease in Scotland: environmental and familial factors;Whalley;Br J Psychiatry Suppl,2001
4. Genotype and Phenotype in Cystic Fibrosis
5. Evidence for three loci modifying age-at-onset of Alzheimer’s disease in early-onset PSEN2 families;Marchani;Am J Med Genet B Neuropsychiatr Genet,2010
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