A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia
Top Cited Papers
- 1 January 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (1), 191-199
- https://doi.org/10.1086/345488
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Ataxia and Paroxysmal Dyskinesia in Mice Lacking Axonally Transported FGF14Neuron, 2002
- Hydrophobic Core Manipulations in Ribonuclease T1Biochemistry, 2001
- Clinical and genetic analysis of 4 Mexican families with spinocerebellar ataxia type 10Annals of Neurology, 2001
- Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10Nature Genetics, 2000
- Enhanced genome annotation using structural profiles in the program 3D-PSSM 1 1Edited by J. ThorntonJournal of Molecular Biology, 2000
- An Unstable Trinucleotide-Repeat Region on Chromosome 13 Implicated in Spinocerebellar Ataxia: A Common Expansion LocusAmerican Journal of Human Genetics, 2000
- Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development.Proceedings of the National Academy of Sciences, 1996
- Errors in protein structuresNature, 1996
- WHAT IF: A molecular modeling and drug design programJournal of Molecular Graphics, 1990
- A simple salting out procedure for extracting DNA from human nucleated cellsNucleic Acids Research, 1988