HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A missense mutation in exon 1 of the keratin 9 gene in a Japanese patient with "Vörner type" hereditary palmoplantar keratoderma.

AuthorsJun-Ichi Sakabe, Motonobu Nakamura, Yoshiki Tokura
JournalEuropean journal of dermatology : EJD (Eur J Dermatol) 2009 May-Jun Vol. 19 Issue 3 Pg. 286-7 ISSN: 1167-1122 [Print] France
PMID19258236 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Keratin-9
Topics
  • Adult
  • Foot Dermatoses (genetics, pathology)
  • Humans
  • Keratin-9 (genetics)
  • Keratoderma, Palmoplantar, Epidermolytic (genetics, pathology)
  • Male
  • Mutation, Missense
  • Pedigree
  • Skin (pathology)

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: