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Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation

BACKGROUND: Familial progressive hyper- and hypopigmentation (FPHH, MIM 145250) is a rare hereditary skin disorder that is predominantly characterized by progressive, diffuse, partly blotchy hyperpigmented lesions intermingled with scattered hypopigmented spots, lentigines and sometimes Cafe-au-lait...

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Detalles Bibliográficos
Autores principales:	Wang, Jianbo, Li, Weisheng, Zhou, Naihui, Liu, Jingliu, Zhang, Shoumin, Li, Xueli, Li, Zhenlu, Yang, Ziliang, Sun, Miao, Li, Min
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789533/ https://www.ncbi.nlm.nih.gov/pubmed/33407466 http://dx.doi.org/10.1186/s12920-020-00851-5

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