Andersen-Tawil syndrome: New potassium channel mutations and possible phenotypic variation-Reference-Cited by-同舟云学术

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Andersen-Tawil syndrome: New potassium channel mutations and possible phenotypic variation

Published:2005-10-10 Issue:7 Volume:65 Page:1083-1089
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Davies N. P.,Imbrici P.,Fialho D.,Herd C.,Bilsland L. G.,Weber A.,Mueller R.,Hilton-Jones D.,Ealing J.,Boothman B. R.,Giunti P.,Parsons L. M.,Thomas M.,Manzur A. Y.,Jurkat-Rott K.,Lehmann-Horn F.,Chinnery P. F.,Rose M.,Kullmann D. M.,Hanna M. G.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 76 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. Phenotypic Variability of Andersen–Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene—A New Family Case Report;Biomolecules;2024-04-22

2. Pediatric neuromuscular channelopathies;Handbook of Clinical Neurology;2024

3. Andersen-Tawil syndrome;Handbook of Clinical Neurology;2024

4. Diagnostics in skeletal muscle channelopathies;Expert Review of Molecular Diagnostics;2023-11-29

5. Muscle channelopathies: A review;Annals of the Child Neurology Society;2023-10-10

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