Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis
- 23 March 2004
- journal article
- case report
- Published by Springer Nature in Journal of Human Genetics
- Vol. 49 (4) , 223-225
- https://doi.org/10.1007/s10038-004-0135-6
Abstract
Journal of Human Genetics, official journal of the Japan Society of Human Genetics, publishes original articles and reviews on all aspects of human genetics, including medical genetics and genomicsKeywords
This publication has 4 references indexed in Scilit:
- Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis☆Genomics, 2003
- TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteinsBMC Genomics, 2003
- A New Germline Mutation of the PTCH Gene in a Japanese Patient with Nevoid Basal Cell Carcinoma Syndrome Associated with MeningiomaJapanese Journal of Clinical Oncology, 2003
- Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformisNature Genetics, 2002