HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.

AuthorsDimitra Kiritsi, Ioana Cosgarea, Claus-Werner Franzke, Hauke Schumann, Vinzenz Oji, Jürgen Kohlhase, Leena Bruckner-Tuderman, Cristina Has
JournalThe Journal of investigative dermatology (J Invest Dermatol) Vol. 130 Issue 6 Pg. 1741-6 (Jun 2010) ISSN: 1523-1747 [Electronic] United States
PMID20164844 (Publication Type: Letter, Research Support, Non-U.S. Gov't)
Chemical References
  • transglutaminase 5
  • Transglutaminases
Topics
  • Adolescent
  • Adult
  • Blister (genetics, pathology)
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Diagnosis, Differential
  • Epidermolysis Bullosa (diagnosis, genetics, pathology)
  • Erythema (genetics, pathology)
  • Humans
  • Infant
  • Infant, Newborn
  • Mutation, Missense (genetics)
  • Skin (pathology)
  • Skin Aging (genetics, pathology)
  • Skin Diseases (diagnosis, genetics, pathology)
  • Syndrome
  • Transglutaminases (genetics)
  • Young Adult

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: