Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity-Reference-Cited by-同舟云学术

Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity

Published:2017-06 Issue:3 Volume:92 Page:329-333
ISSN:0365-0596
Container-title:Anais Brasileiros de Dermatologia
language:
Short-container-title:An. Bras. Dermatol.

Author:

Xiao-Kai Fang¹,Yue-Xi He¹,Yan-Jia Li²,Li-Rong Chen²,He-Peng Wang²,Qing Sun¹

Affiliation:

1. Shandong University, China

2. Hebei Medical University, China

Publisher

FapUNIFESP (SciELO)

Subject

Dermatology

Link

http://www.scielo.br/pdf/abd/v92n3/0365-0596-abd-92-03-0329.pdf

Reference19 articles.

1. Familial progressive hyperpigmentation;Chernosky ME;Arch Dermatol,1971

2. Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family;Zhang C;Eur J Dermatol,2006

3. Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in south-east Germany;Zanardo L;Acta Derm Venereol,2004

4. KITLG mutations cause familial progressive hyper- and hypopigmentation;Amyere M;J Invest Dermatol,2011

5. Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation;Wang ZQ;Am J Hum Genet,2009

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1. Cutaneous findings in Fanconi anemia;Journal of the American Academy of Dermatology;2021-11

2. Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation;BMC Medical Genomics;2021-01-06

3. Café noir spots: a feature of familial progressive hyper‐ and hypopigmentation;Journal of the European Academy of Dermatology and Venereology;2019-10-24