Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)-Reference-Cited by-同舟云学术

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Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

Published:1994-11 Issue:5 Volume:94 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Plassart Emmanuelle,Elbaz Alexis,Santos JoseVale,Reboul Jocelyne,Lapie Pascale,Chauveau Dominique,Jurkat-Rott Karin,Guimaraes Joao,Saudubray Jean-Marie,Weissenbach Jean,Lehmann-Horn Frank,Fontaine Bertrand

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00211025.pdf

Cited by 33 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. Familial Hypokalemic Periodic Paralysis: Case Report;Eurasian Journal of Family Medicine;2019-06-26

2. Skeletal Muscle Channelopathies;Neurotherapeutics;2018-10

3. Diverse phenotype of hypokalaemic periodic paralysis within a family;Practical Neurology;2017-09-28

4. Cav1.1 Channel and Hypokalemic Periodic Paralysis;Pathologies of Calcium Channels;2013-11-09

5. Disorders of Skeletal Muscle Membrane Excitability: Myotonia Congenita, Paramyotonia Congenita, Periodic Paralysis, and Related Syndromes;Neuromuscular Disorders in Clinical Practice;2013-04-26

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