Identification of three novel mutations in the gene for CuZn superoxide dismutase in patients with familial amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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Identification of three novel mutations in the gene for CuZn superoxide dismutase in patients with familial amyotrophic lateral sclerosis

Published:1995-09 Issue:5 Volume:5 Page:353-357
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Sapp Peter C,Rosen Daniel R,Hosler Betsy A,Esteban Jesus,McKenna-Yasek Diane,O'regan Jeremiah P,Horvitz H.Robert,Brown Robert H

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology and ethical issues in management;Tandan;Annals Neurol,1985

2. Amyotrophic lateral sclerosis: Part 2. Etiopathogenesis;Tandan;Annals Neurol,1985

3. Familial adult motor neuron disease: amyotrophic lateral sclerosis;Mulder;Neurology,1986

4. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers;Rosen;Am J Med Genet,1994

5. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity;Siddique;N Engl J Med,1991

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3. Case report: Flail leg syndrome in familial amyotrophic lateral sclerosis with L144S SOD1 mutation;Frontiers in Neurology;2023-03-22

4. Analysis of SOD1 variants in Chinese patients with familial amyotrophic lateral sclerosis;QJM: An International Journal of Medicine;2023-01-20

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