Schöpf-Schulz-Passarge Syndrome: Previously Unreported WNT10A Genotype and Phenotypes in 9 Family Members

Authors

  • Corinna E. Zimmermann
  • Muhidien Soufi
  • Volker Ruppert
  • Juergen R. Schaefer
  • Helmut von Domarus

DOI:

https://doi.org/10.2340/00015555-3055

Abstract

Abstract is missing (Short communication)

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Published

2018-10-04

How to Cite

Zimmermann, C. E., Soufi, M., Ruppert, V., Schaefer, J. R., & von Domarus, H. (2018). Schöpf-Schulz-Passarge Syndrome: Previously Unreported WNT10A Genotype and Phenotypes in 9 Family Members. Acta Dermato-Venereologica, 99(1), 113–114. https://doi.org/10.2340/00015555-3055

Issue

Vol. 99 No. 1 (2019): January

Section

Short Communication

License

Copyright (c) 2018 Corinna E. Zimmermann, Muhidien Soufi, Volker Ruppert, Juergen R. Schaefer, Helmut von Domarus

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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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