Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families-Reference-Cited by-同舟云学术

Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families

Published:2020-10-08 Issue:2 Volume:34 Page:174-178
ISSN:1755-1471
Container-title:Pigment Cell & Melanoma Research
language:en
Short-container-title:Pigment Cell Melanoma Res.

Author:

Araki Yuta¹^ORCID,Okamura Ken¹^ORCID,Saito Toru¹,Matsumoto Kazuhiko²^ORCID,Natsuga Ken³^ORCID,Nishimoto Junko⁴,Funasaka Yoko⁵,Togawa Yaei⁶^ORCID,Suzuki Tamio¹^ORCID

Affiliation:

1. Department of Dermatology, Faculty of Medicine Yamagata University Yamagata Japan

2. Department of Dermatology Shinshu University School of Medicine Matsumoto Japan

3. Department of Dermatology Hokkaido University Graduate School of Medicine Sapporo Japan

4. Department of Dermatology, Faculty of Medicine University of Miyazaki Miyazaki Japan

5. Department of Dermatology Nippon Medical School Tokyo Japan

6. Department of Dermatology, Graduate School of Medicine Chiba University Chiba Japan

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pcmr.12930

Reference20 articles.

1. Generalized Lentiginosis in Two Children Lacking Systemic Associations: Case Report and Review of the Literature

2. Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma

3. SASH1 promotes melanin synthesis and migration via suppression of TGF‐beta1 secretion in melanocytes resulting in pathologic hyperpigmentation;Cui H.;International Journal of Biological Sciences,2020

4. STAR: ultrafast universal RNA-seq aligner

5. The differential diagnosis of familial lentiginosis syndromes

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