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Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss.
De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper- and Hypo-pigmentation (FPHH).
Familial progressive hyper- and hypopigmentation caused by a novel mutation in site II of the KITLG gene.
Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation.
Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation.