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Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family

  • Published:2017-04-13 Issue:8 Volume:44 Page:e184-e185
  • ISSN:0385-2407
  • Container-title:The Journal of Dermatology
  • language:en
  • Short-container-title:J Dermatol

Author:

Yoshida Kazue1ORCID,Hayashi Ryota2,Shimomura Yutaka2,Niizeki Hironori1ORCID

Affiliation:

1. Department of Dermatology; National Center for Child Health and Development; Tokyo Japan

2. Division of Dermatology; Niigata University Graduate School of Medical and Dental Sciences; Niigata Japan

Funder

National Center for Child Health and Development

“Research on Measures for Intractable Diseases”

Ministry of Health, Labour and Welfare

Publisher

Wiley

Subject

Dermatology,General Medicine

Cited by 4 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. Update of recent findings in genetic hair disorders;The Journal of Dermatology;2021-10-21

2. Genetic Hair Disorders: A Review;Dermatology and Therapy;2019-07-22

3. Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report;European Journal of Dermatology;2018-05

4. Hereditary Hair Diseases (part 1);Nishi Nihon Hifuka;2018-04-01
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