HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A novel frameshift mutation in keratin 16 underlies pachyonychia congenita with focal palmoplantar keratoderma.

AuthorsL-H Cao, Y Luo, W Wen, W-L Liu, L Jiang, C Chen, C-Y Ji, X Zhang
JournalThe British journal of dermatology (Br J Dermatol) Vol. 165 Issue 5 Pg. 1145-7 (Nov 2011) ISSN: 1365-2133 [Electronic] England
PMID21668426 (Publication Type: Case Reports, Letter, Research Support, Non-U.S. Gov't)
Chemical References
  • Keratin-16
Topics
  • Frameshift Mutation (genetics)
  • Humans
  • Keratin-16 (genetics)
  • Keratoderma, Palmoplantar (genetics)
  • Male
  • Middle Aged
  • Pachyonychia Congenita (genetics)
  • Pedigree
  • Phenotype

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: