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Article

V876E mutation in CACNA1S gene associated with severe hypokalemic periodic paralysis in a Chinese woman.

Journal of the Formosan Medical Association = Taiwan yi zhi - 1 Apr 2015

Yang Hongbo, Zhang Huabing, Xing Xiaoping

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PMID: 23948435
DOI: 10.1016/j.jfma.2013.07.007

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V876E mutation in CACNA1S gene associated with severe hypokalemic periodic paralysis in a Chinese woman.PMID 23948435Read ↗

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The R900S mutation in CACNA1S associated with hypokalemic periodic paralysis.Semantic proximity Read ↗

The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S.Semantic proximity Read ↗

A novel CACNA1S gene variant in a child with hypokalemic periodic paralysis: a case report and literature review.Semantic proximity Read ↗

Novel CACNA1S Mutation c.3491 A>C in Hypokalemic Periodic Paralysis: First Report with Functional Validation.Semantic proximity Read ↗

A novel mutation in CACNA1S gene associated with hypokalemic periodic paralysis which has a gender difference in the penetrance.Semantic proximity Read ↗

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.Semantic proximity Read ↗

[R1239H mutation of CACNA1S gene in a Chinese family with hypokalaemic periodic paralysis].Semantic proximity Read ↗

Clinical and molecular analysis of chinese patients with thyrotoxic periodic paralysis.Semantic proximity Read ↗

A Novel CLCN1 Gene Mutation Associated with Hypokalemic Periodic Paralysis in a Pregnant Woman.Semantic proximity Read ↗

[Screening of genetic mutations in a Chinese pedigree affected with hypokalemic periodic paralysis].Semantic proximity Read ↗

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