Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability-Reference-Cited by-同舟云学术

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

Published:2000-10 Issue:4 Volume:48 Page:647-656
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Eunson L. H.,Rea R.,Zuberi S. M.,Youroukos S.,Panayiotopoulos C. P.,Liguori R.,Avoni P.,McWilliam R. C.,Stephenson J. B. P.,Hanna M. G.,Kullmann D. M.,Spauschus A.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference34 articles.

1. Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders

2. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system

3. Very large radio surveys of the sky

4. Phenotype variation and newcomers in ion channel disorders

5. Members of the RCK potassium channel family are differentially expressed in the rat nervous system.

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