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Pharmaceuticals (Basel, Switzerland)|May 4, 2026
Analytical and Clinical Validation of Action PharmaKitDx: A Comprehensive NGS Panel for the Identification of Pharmacogenetic Variants in Diverse PopulationsLuis Ramudo-Cela, Marta Izquierdo-García, María Dolores-Sequedo, et al.Human Mutation|April 27, 2011
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing lossMichael S Hildebrand, Matías Morín, Nicole C Meyer, et al.American Journal of Human Genetics|November 3, 2015
Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2Celia Zazo Seco, Luciana Serrão de Castro, Josephine W van Nierop, et al.Pageof 3