Effect on splicing of a silent FGFR2 mutation in Crouzon syndrome
- 1 March 1995
- journal article
- other
- Published by Springer Nature in Nature Genetics
- Vol. 9 (3) , 232-233
- https://doi.org/10.1038/ng0395-232
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Craniofacial syndromes: no such thing as a single gene diseaseNature Genetics, 1995
- Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2Nature Genetics, 1994
- Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeNature Genetics, 1994
- RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expressionNucleic Acids Research, 1987