The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear Implantees
Charlotte M. Chiong(Philippine General Hospital), Regie Lyn P. Santos‐Cortez(University of Colorado Anschutz Medical Campus), Celina Ann M. Tobias-Grasso(MED-EL (Austria)), Karen L. Mohlke(University of North Carolina at Chapel Hill), Nanette L. Mayol(Population Council), Suzanne M. Leal(Baylor College of Medicine), Anushree Acharya(Baylor College of Medicine), Talitha Karisse L. Yarza(University of the Philippines Manila), Eva Maria Cutiongco‐de la Paz(Philippine Heart Center), Ma. Rina T. Reyes‐Quintos(University of the Philippines Manila)
Cited by 11
Related Papers
A second generation human haplotype map of over 3.1 million SNPs
|Nature|2007|4.6k
Single-nucleotide polymorphism in the human mu opioid receptor gene alters β-endorphin binding and activity: Possible implications for opiate addiction
|Proceedings of the National Academy of Sciences|1998|1.1k
Common variants in the GDF5-UQCC region are associated with variation in human height
|Nature Genetics|2008|401
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1
|Nature Genetics|2011|219
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
|Nature Communications|2022|191