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Familial progressive hyper‐ and hypopigmentation caused by a novel mutation in site II of the KITLG gene

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Bibliographic Details
Published in:	Journal of dermatology 2021-09, Vol.48 (9), p.e462-e463
Main Authors:	Liu, Zhenfeng, Zhu, Zhenlai, Luo, Junjie, Yang, Bin
Format:	Article
Language:	English
Subjects:	Albinism, Oculocutaneous Humans Hyperpigmentation - diagnosis Hyperpigmentation - genetics Hypopigmentation - diagnosis Hypopigmentation - genetics Male Mutation Pigmentation Stem Cell Factor - genetics
Citations:	Items that this one cites
Online Access:	Get full text
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