A calcium channel mutation causing hypokalemic periodic paralysis-Reference-Cited by-同舟云学术

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A calcium channel mutation causing hypokalemic periodic paralysis

Published:1994 Issue:8 Volume:3 Page:1415-1419
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Jurkat-Rott Karln,Lehmann-Horn Frank,Elbaz Alexis,Heine Roland,Gregg Ronald G.,Hogan Kirk,Powers Patricia A.,Laple Pascale,Vale-Santos José E.,Weissenbach Jean,Fontaine Bertrand

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/8/1415/1473902/3-8-1415.pdf

Cited by 300 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. Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene;Journal of Neuromuscular Diseases;2024-07-02

2. Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients;Orphanet Journal of Rare Diseases;2024-04-12

3. A Rare Case of Hypokalemic Periodic Paralysis With Acute Urinary Retention: Diagnosis and Management;Cureus;2024-01-24

4. Periodic paralysis;Handbook of Clinical Neurology;2024

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

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