Literature DB >> 26083144

Hypokalemic periodic paralysis: an omega pore mutation affects inactivation.

Roope Männikkö1, Dimitri M Kullmann.   

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Year:  2015        PMID： 26083144      PMCID： PMC4594596          DOI： 10.1080/19336950.2015.1062325

Source DB:  PubMed          Journal:  Channels (Austin)        ISSN： 1933-6950            Impact factor:   2.581


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  6 in total

Review 1.  Voltage-sensor mutations in channelopathies of skeletal muscle.

Authors:  Stephen C Cannon
Journal:  J Physiol       Date:  2010-02-15       Impact factor: 5.182

2.  Depolarization-activated gating pore current conducted by mutant sodium channels in potassium-sensitive normokalemic periodic paralysis.

Authors:  Stanislav Sokolov; Todd Scheuer; William A Catterall
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-03       Impact factor: 11.205

3.  Myasthenic syndrome caused by mutation of the SCN4A sodium channel.

Authors:  Akira Tsujino; Chantal Maertens; Kinji Ohno; Xin-Ming Shen; Taku Fukuda; C Michael Harper; Stephen C Cannon; Andrew G Engel
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-23       Impact factor: 11.205

4.  Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.

Authors:  E Matthews; R Labrum; M G Sweeney; R Sud; A Haworth; P F Chinnery; G Meola; S Schorge; D M Kullmann; M B Davis; M G Hanna
Journal:  Neurology       Date:  2008-12-31       Impact factor: 9.910

5.  Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutation.

Authors:  James R Groome; Karin Jurkat-Rott; Frank Lehmann-Horn
Journal:  Channels (Austin)       Date:  2014       Impact factor: 2.581

6.  NaV1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery.

Authors:  James R Groome; Frank Lehmann-Horn; Chunxiang Fan; Markus Wolf; Vern Winston; Luciano Merlini; Karin Jurkat-Rott
Journal:  Brain       Date:  2014-02-18       Impact factor: 13.501
  6 in total

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