Associated Papers
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
Mosaicism for a KITLG Mutation in Linear and Whorled Nevoid Hypermelanosis.
Sorlin A et al.
The Journal of Investigative Dermatology, 2017
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