Café noir spots: a feature of familial progressive hyper‐ and hypopigmentation-Reference-Cited by-同舟云学术

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Café noir spots: a feature of familial progressive hyper‐ and hypopigmentation

Published:2019-10-24 Issue:2 Volume:34 Page:
ISSN:0926-9959
Container-title:Journal of the European Academy of Dermatology and Venereology
language:en
Short-container-title:J Eur Acad Dermatol Venereol

Author:

Gülseren D.¹^ORCID,Güleray N.²,Akgün‐Doğan Ö.³,Şimşek‐Kiper P.Ö.³,Utine E.G.³,Alikaşifoğlu M.²,Ersoy‐Evans S.¹

Affiliation:

1. Department of Dermatology Hacettepe University, School of Medicine Ankara Turkey

2. Department of Medical Genetics School of Medicine Hacettepe University Ankara Turkey

3. Department of Pediatrics Department of Pediatric Genetics School of Medicine Hacettepe University Ankara Turkey

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jdv.15968

Reference10 articles.

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

2. KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation

3. Hereditary Congenital Hypopigmented and Hyperpigmented Macules

4. Familial progressive hypo- and hyperpigmentation: A variant case

5. The LEOPARD (multiple lentigines) syndrome revisited;Gorlin RJ;Birth Defects Orig Artic Ser,1971

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 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

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