Keratoderma-Deafness-Mucocutaneous Syndrome Associated with Phe142Leu in the GJB2 Gene

Authors

  • Liliana Guerra
  • Fabio Bergamo
  • Maria Rosaria D'Apice
  • Francesco Angelucci
  • Stefano Di Girolamo
  • Letizia Camerota
  • Rosanna Monetta
  • Giorgio Annessi
  • Daniele Castiglia
  • Giuseppe Novelli
  • Mauro Paradisi
  • Francesco Brancati

DOI:

https://doi.org/10.2340/00015555-3291

Keywords:

Connexin 26, GJB2, palmoplantar keratoderma, mucocutaneous, deafness, syndrome

Abstract

Abstract is missing (Short communication)

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Published

2019-09-23

How to Cite

Guerra, L., Bergamo, F., D’Apice, M. R., Angelucci, F., Di Girolamo, S., Camerota, L., Monetta, R., Annessi, G., Castiglia, D., Novelli, G., Paradisi, M., & Brancati, F. (2019). Keratoderma-Deafness-Mucocutaneous Syndrome Associated with Phe142Leu in the GJB2 Gene. Acta Dermato-Venereologica, 99(12), 1192–1194. https://doi.org/10.2340/00015555-3291

Issue

Vol. 99 No. 12 (2019): November

Section

Short Communication

License

Copyright (c) 2019 Liliana Guerra, Fabio Bergamo, Maria Rosaria D'Apice, Francesco Angelucci, Stefano Di Girolamo, Letizia Camerota, Rosanna Monetta, Giorgio Annessi, Daniele Castiglia, Giuseppe Novelli, Mauro Paradisi, Francesco Brancati

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