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European Journal of Dermatology

, Volume 28, Issue 3, pp 406–407 | Cite as

Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report

  • Yurika Masuda
  • Taisuke Ito
  • Yutaka Shimomura
  • Masaaki Ogai
  • Jun-Ichi Sakabe
  • Yoshiki Tokura
Correspondence
  • 6 Downloads

References

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    Ito T, Shimomura Y, Ogai M, Sakabe J, Tokura Y. Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis. J Dermatol 2013; 40: 278–80.CrossRefPubMedGoogle Scholar
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    Yoshida K, Hayashi R, Shimomura Y, Niizeki H. Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family. J Dermatol 2017; 44:e184–5.CrossRefGoogle Scholar
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Copyright information

© John Libbey Eurotext 2018

Authors and Affiliations

  • Yurika Masuda
    • 1
  • Taisuke Ito
    • 1
  • Yutaka Shimomura
    • 2
  • Masaaki Ogai
    • 3
  • Jun-Ichi Sakabe
    • 4
  • Yoshiki Tokura
    • 1
  1. 1.Department of DermatologyHamamatsu University School of MedicineHamamatsuJapan
  2. 2.Department of DermatologyYamaguchi University Faculty of Medicine and Health SciencesYamaguchiJapan
  3. 3.Department of DermatologySeirei Hamamatsu General HospitalShizuokaJapan
  4. 4.Institute of Medical BiologyAgency for Science, Technology and Research (A*STAR)Singapore CitySingapore

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