A Novel KIT Gene Missense Mutation in a Japanese Family with Piebaldism
- 1 August 1998
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 111 (2) , 337-338
- https://doi.org/10.1046/j.1523-1747.1998.00269.x
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Mutations in the Ligand-Binding Domain of the Kit Receptor: An Uncommon Site in Human PiebaldismJournal of Investigative Dermatology, 1996
- A 12-bp deletion ( 7818del12 ) in the c-kit protooncogene in a large Italian kindred with piebaldismHuman Mutation, 1995
- Molecular Basis of Human PiebaldismJournal of Investigative Dermatology, 1994
- Novel Mutations of the KIT (Mast/Stem Cell Growth Factor Receptor) Proto-Oncogene in Human PiebaldismJournal of Investigative Dermatology, 1993
- Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.Proceedings of the National Academy of Sciences, 1991