The genetic basis of tuberous sclerosis
- 1 July 1998
- journal article
- review article
- Published by Elsevier BV in Molecular Medicine Today
- Vol. 4 (7), 313-319
- https://doi.org/10.1016/s1357-4310(98)01245-3
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Loss of heterozygosity in tuberous sclerosis hamartomas.Journal of Medical Genetics, 1996
- Novel Mutations Detected in the TSC2 Hene From Both Sporadic and Familial TSC PatientsHuman Molecular Genetics, 1996
- Identification of Tuberin, the Tuberous Sclerosis-2 Product. TUBERIN POSSESSES SPECIFIC Rap1GAP ACTIVITYJournal of Biological Chemistry, 1995
- A germline insertion in the tuberous sclerosis (Tsc2) gene gives rise to the Eker rat model of dominantly inherited cancerNature Genetics, 1995
- Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13Annals of Human Genetics, 1994
- Variability of expression in tuberous sclerosis.Journal of Medical Genetics, 1993
- Non-penetrance in tuberous sclerosis.Journal of Medical Genetics, 1991
- 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
- A Dominant Gene for Renal Adenomas in the RatNature, 1961