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Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.
- Source :
-
Human mutation [Hum Mutat] 1998; Vol. Suppl 1, pp. S85-7. - Publication Year :
- 1998
- Subjects :
- Adolescent
Adult
Base Sequence
DNA chemistry
DNA genetics
DNA Mutational Analysis
Family Health
Female
GTPase-Activating Proteins
Humans
Male
Mutation
Pedigree
Polymorphism, Single-Stranded Conformational
Protein Structure, Tertiary
Repressor Proteins chemistry
Sequence Deletion
Tuberous Sclerosis Complex 2 Protein
Tumor Suppressor Proteins
Proteins genetics
Repressor Proteins genetics
Tuberous Sclerosis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1059-7794
- Volume :
- Suppl 1
- Database :
- MEDLINE
- Journal :
- Human mutation
- Publication Type :
- Academic Journal
- Accession number :
- 9452050
- Full Text :
- https://doi.org/10.1002/humu.1380110129