HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A case of erythrokeratodermia variabilis with connexin 31 gene mutation (Cx31F137L).

AuthorsTiago Torres, Gloria Velho, Madalena Sanches, Manuela Selores
JournalInternational journal of dermatology (Int J Dermatol) Vol. 51 Issue 4 Pg. 494-6 (Apr 2012) ISSN: 1365-4632 [Electronic] England
PMID21913904 (Publication Type: Case Reports, Letter)
Chemical References
  • Connexins
  • GJB3 protein, human
Topics
  • Connexins (genetics)
  • Erythrokeratodermia Variabilis (diagnosis, drug therapy, genetics)
  • Genetic Testing
  • Humans
  • Infant
  • Male
  • Mutation

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: