SOD1 missense mutation in an Italian family with ALS-Reference-Cited by-同舟云学术

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SOD1 missense mutation in an Italian family with ALS

Published:1994-02-01 Issue:2 Volume:44 Page:347-347
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Rainero I.,Pinessi L.,Tsuda T.,Vignocchi M. G.,Vaula G.,Calvi L.,Cerrato P.,Rossi B.,Bergamini L.,McLachlan D. R. C.,St. George-Hyslop P. H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 63 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The G41D mutation in SOD1-related amyotrophic lateral sclerosis exhibits phenotypic heterogeneity among individuals;Medicine;2022-02-11

2. Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype;Frontiers in Genetics;2021-11-17

3. A Novel Variant in Superoxide Dismutase 1 Gene (p.V119M) in Als Patients with Pure Lower Motor Neuron Presentation;Genes;2021-09-29

4. Locomotor analysis identifies early compensatory changes during disease progression and subgroup classification in a mouse model of amyotrophic lateral sclerosis;NEURAL REGEN RES;2017

5. Neuronal Mitochondria as a Target for the Discovery and Development of New Therapeutics;The Functions, Disease-Related Dysfunctions, and Therapeutic Targeting of Neuronal Mitochondria;2015-09-25

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