DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)-Reference-Cited by-同舟云学术

DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

Published:2004-06 Issue:6 Volume:74 Page:1128-1135
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Chen Ying-Zhang,Bennett Craig L.,Huynh Huy M.,Blair Ian P.,Puls Imke,Irobi Joy,Dierick Ines,Abel Annette,Kennerson Marina L.,Rabin Bruce A.,Nicholson Garth A.,Auer-Grumbach Michaela,Wagner Klaus,De Jonghe Peter,Griffin John W.,Fischbeck Kenneth H.,Timmerman Vincent,Cornblath David R.,Chance Phillip F.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

1. A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34;Blair;Neurogenetics,2000

2. Direct interaction of SMN with dp103, a putative RNA helicase: a role for SMN in transcription regulation?;Campbell;Hum Mol Genet,2000

3. Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34;Chance;Am J Hum Genet,1998

4. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene;Date;Nat Genet,2001

5. Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?;De Jonghe;Brain,2002

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