A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling-Reference-Cited by-同舟云学术

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A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling

Published:2015-04 Issue: Volume: Page:635
ISSN:1178-203X
Container-title:Therapeutics and Clinical Risk Management
language:en
Short-container-title:TCRM

Author:

Li Cheng-Rang,Jia Wei-Xue,Xiao Xue-Min,Wu Jian-Bing,Ma Yi-Ping,Ge Yi-Ping,Li Qi,Mao Qiu-Xia

Publisher

Informa UK Limited

Subject

Chemical Health and Safety,Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics,Safety Research,General Medicine

Cited by 7 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. Piebaldism with Neurofibromatosis-1 with Skeletal Anomalies in Two Successive Generations;Indian Journal of Paediatric Dermatology;2023

2. KIT gene mutation causing piebaldism associated with multiple Café Au-Lait like macules and freckling: Delineating a cause of this coexistence;Indian Dermatology Online Journal;2023

3. CHEK2 Mutation in Patient with Multiple Endocrine Glands Tumors. Case Report;International Journal of Environmental Research and Public Health;2020-06-18

4. Piebaldism: An Iranian case report carrying minor allele at rs999020 and rs1008658 SNPs of KIT gene;Gene Reports;2019-12

5. Piebaldism Associated with Café-au-lait Macules and Intertriginous Freckling: A Case Report and Review of the Literature;Annals of Dermatology;2019

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