Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation-Reference-Cited by-同舟云学术

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Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation

Published:2020-03-18 Issue:6 Volume:47 Page:669-672
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Kato Maki¹,Yagami Akiko²,Tsukamoto Tetsuya³,Shinkai Yasuko¹,Kato Takema¹,Kurahashi Hiroki¹^ORCID

Affiliation:

1. Division of Molecular Genetics Institute for Comprehensive Medical Science Fujita Health University Toyoake Japan

2. Departments of Department of Dermatology Fujita Health University School of Medicine Toyoake Japan

3. Department of Diagnostic Pathology Fujita Health University School of Medicine Toyoake Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Agency for Medical Research and Development

Ministry of Health, Labour and Welfare

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15313

Reference10 articles.

1. KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation

2. Structural basis for stem cell factor–KIT signaling and activation of class III receptor tyrosine kinases

3. Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations inKITLG

4. Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novelKITLGmutation

5. Using SIFT and PolyPhen to Predict Loss-of-Function and Gain-of-Function Mutations

Cited by 5 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. Therapeutic modulation of KIT ligand in melanocytic disorders with implications for mast cell diseases;Experimental Dermatology;2024-05

2. Integration of transcriptomics and metabolomics reveals amelanism mechanism of Oscar Astronotus ocellatus (Agassiz, 1831);Hydrobiologia;2022-09-12

3. De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper‐ and Hypo‐pigmentation (FPHH);Molecular Genetics & Genomic Medicine;2021-10-30

4. Familial progressive hyper‐ and hypopigmentation caused by a novel mutation in site II of the KITLG gene;The Journal of Dermatology;2021-06-11

5. 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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