Three novel COLQ mutations and variation of phenotypic expressivity due to G240X-Reference-Cited by-同舟云学术

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Three novel COLQ mutations and variation of phenotypic expressivity due to G240X

Published:2002-02-26 Issue:4 Volume:58 Page:603-609
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Shapira Y.A.,Sadeh M.E.,Bergtraum M.P.,Tsujino A.,Ohno K.,Shen X.-M.,Brengman J.,Edwardson S.,Matoth I.,Engel A.G.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 48 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. Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes;Neurology Clinical Practice;2024-06

2. Pharmacological Treatments for Congenital Myasthenic Syndromes Caused by COLQ Mutations;Current Neuropharmacology;2023-07

3. Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families;Revue Neurologique;2023-06

4. COLQ-related congenital myasthenic syndrome: An integrative view;neurogenetics;2023-05-25

5. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review;International Journal of Molecular Sciences;2023-02-13

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