Associated Papers
Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss.
Vona B et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2022
35543077 (PubMed )
Supplement: JDV-36-1606-s001.xlsx › Sheet1
Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation.
Wang J et al.
Bmc Medical Genomics, 2021
Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2.
Zazo Seco C et al.
American Journal of Human Genetics, 2015
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