A Point Mutation in an Intronic Branch Site Results in Aberrant Splicing of COL5A1 and in Ehlers-Danlos Syndrome Type II in Two British Families
- 1 August 1998
- journal article
- case report
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (2) , 390-398
- https://doi.org/10.1086/301948
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome.Journal of Medical Genetics, 1996
- A splice-junction mutation in the region of COL5A1 that codes for the carboxyl propeptide of pro alpha 1(V) chains results in the gravis form of the Ehlers-Danlos syndrome (type I)Human Molecular Genetics, 1996
- A translocation interrupts the COL5A1 gene in a patient with Ehlers–Danlos syndrome and hypomelanosis of ItoNature Genetics, 1996
- The Gene Encoding Collagen α1(V) (COL5A1) Is Linked to Mixed Ehlers-Danlos Syndrome Type I/IIJournal of Investigative Dermatology, 1996
- Complete Structural Organization of the Human α1(V) Collagen Gene (COL5A1): Divergence from the Conserved Organization of Other Characterized Fibrillar Collagen GenesGenomics, 1995
- Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assemblyNature Genetics, 1995
- Human collagen gene COL5A1 maps to the q34.2→q34.3 region of chromosome 9, near the locus for nail-patella syndromeGenomics, 1992
- Mammalian pre-mRNA branch site selection by U2 snRNP involves base pairing.Genes & Development, 1989
- The role of the mammalian branchpoint sequence in pre-mRNA splicing.Genes & Development, 1988
- Articular mobility in an African population.Annals of the Rheumatic Diseases, 1973