Expanding the Clinical Phenotype Associated WithELOVL4Mutation-Reference-Cited by-同舟云学术

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Expanding the Clinical Phenotype Associated WithELOVL4Mutation

Published:2014-04-01 Issue:4 Volume:71 Page:470
ISSN:2168-6149
Container-title:JAMA Neurology
language:en
Short-container-title:JAMA Neurol

Author:

Cadieux-Dion Maxime¹,Turcotte-Gauthier Maude¹,Noreau Anne²,Martin Caroline¹,Meloche Caroline¹,Gravel Micheline¹,Drouin Christian Allen³,Rouleau Guy A.²,Nguyen Dang Khoa¹,Cossette Patrick¹

Affiliation:

1. Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Notre Dame Hospital, University of Montreal, Montreal, Quebec, Canada

2. Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada

3. Department of Dermatology, Grand Portage Hospital, Rivière du Loup, Quebec, Canada

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

Cited by 109 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. A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex;Neuroscience Bulletin;2024-06-13

2. The Spinocerebellar Ataxia 34-Causing W246G ELOVL4 Mutation Does Not Alter Cerebellar Neuron Populations in a Rat Model;The Cerebellum;2024-06-08

3. Potential Clinical Benefit of Very Long Chain Fatty Acid Supplementation in Spinocerebellar Ataxia Type 34;The Cerebellum;2024-05-21

4. Disorders of fatty acid homeostasis;Journal of Inherited Metabolic Disease;2024-05

5. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19

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