Complete Inactivation of the TSC2 Gene Leads to Formation of Hamartomas
- 1 December 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (6) , 1790-1794
- https://doi.org/10.1086/302648
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34Science, 1997
- Intragenic Tsc2 Somatic Mutations as Knudson's Second Hit in Spontaneous and Chemically Induced Renal Carcinomas in the Eker Rat ModelJapanese Journal of Cancer Research, 1997
- Loss of heterozygosity in tuberous sclerosis hamartomas.Journal of Medical Genetics, 1996
- A cross sectional study of renal involvement in tuberous sclerosis.Journal of Medical Genetics, 1996
- Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band l6p13 occurs in sporadic as well as TSC‐associated renal angiomyolipomasGenes, Chromosomes and Cancer, 1995
- A germline insertion in the tuberous sclerosis (Tsc2) gene gives rise to the Eker rat model of dominantly inherited cancerNature Genetics, 1995
- Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patientsNature Genetics, 1994
- Identification and characterization of the tuberous sclerosis gene on chromosome 16Cell, 1993
- Genetic aspects of tuberous sclerosis in the west of Scotland.Journal of Medical Genetics, 1989
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971