CLCN1 Mutations in Czech Patients with Myotonia Congenita, In Silico Analysis of Novel and Known Mutations in the Human Dimeric Skeletal Muscle Chloride Channel-Reference-Cited by-同舟云学术

CLCN1 Mutations in Czech Patients with Myotonia Congenita, In Silico Analysis of Novel and Known Mutations in the Human Dimeric Skeletal Muscle Chloride Channel

Published:2013-12-11 Issue:12 Volume:8 Page:e82549
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Skálová Daniela,Zídková Jana,Voháňka Stanislav,Mazanec Radim,Mušová Zuzana,Vondráček Petr,Mrázová Lenka,Kraus Josef,Réblová Kamila,Fajkusová Lenka

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference50 articles.

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3. Myotonia caused by mutations in the muscle chloride channel gene CLCN1;M Pusch;Hum Mutat,2002

4. Purification, reconstitution, and subunit composition of a voltage-gated chloride channel from Torpedo electroplax;RE Middleton;Biochemistry,1994

5. Homodimeric architecture of a ClC-type chloride ion channel;RE Middleton;Nature,1996

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