Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene

Authors

  • Leila Youssefian
  • Hassan Vahidnezhad
  • Yahya Aghighi
  • Vahid Ziaee
  • Sirous Zeinali
  • Maryam Abiri
  • Jouni Uitto

DOI:

https://doi.org/10.2340/00015555-2459

Abstract

Abstract is missing (Short communication)

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Published

2016-07-27

How to Cite

Youssefian, L., Vahidnezhad, H., Aghighi, Y., Ziaee, V., Zeinali, S., Abiri, M., & Uitto, J. (2016). Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene. Acta Dermato-Venereologica, 97(1), 108–109. https://doi.org/10.2340/00015555-2459

Issue

Vol. 97 No. 1 (2017)

Section

Short Communication

License

Copyright (c) 2016 Leila Youssefian, Hassan Vahidnezhad, Yahya Aghighi, Vahid Ziaee, Sirous Zeinali, Maryam Abiri, Jouni Uitto

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Unless otherwise specified, all Open Access articles are published under CC-BY-NC licences, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for non-commercial purposes, provided proper attribution to the original work.

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