DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)
Top Cited Papers
- 1 June 2004
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 74 (6) , 1128-1135
- https://doi.org/10.1086/421054
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2Nature Genetics, 2004
- Genetic epidemiology of amyotrophic lateral sclerosisClinical Genetics, 2003
- Separable Roles for rent1/hUpf1 in Altered Splicing and Decay of Nonsense TranscriptsScience, 2002
- Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?Brain, 2002
- Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33–q34Annals of Neurology, 2002
- DExD/H Box RNA HelicasesMolecular Cell, 2001
- Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?Human Molecular Genetics, 2000
- Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34American Journal of Human Genetics, 1998
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASEBrain, 1964