A patient suffering from hypokalemic periodic paralysis is deficient in skeletal muscle ATP-sensitive K+ channels

Clinical and Translational Science

Volumn 1, Issue 1, 2008, Pages 71-74

  Jovanovic, Sofija ^a   Du, Qingyou ^a   Mukhopadhyay, Somnath ^b   Swingler, Robert ^a   Buckley, Richard ^a   McEachen, Jane ^c   Jovanović, Aleksandar ^a  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

^b ROYAL ALEXANDRA CHILDREN S HOSPITAL   (United Kingdom)

^c QUEEN MARGARET HOSPITAL   (United Kingdom)

Author keywords

Hypokalemic periodic paralysis; KATP channels; Kir6.2; Skeletal muscle

Indexed keywords

ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; ARGININE; HISTIDINE; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; MESSENGER RNA; INWARDLY RECTIFYING POTASSIUM CHANNEL; POTASSIUM; PRIMER DNA;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN TISSUE; HYPOKALEMIA; HYPOKALEMIC PERIODIC PARALYSIS; IMMUNOPRECIPITATION; MALE; MUSCLE WEAKNESS; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN DEFICIENCY; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SARCOLEMMA; SKELETAL MUSCLE; WESTERN BLOTTING; BIOSYNTHESIS; CASE CONTROL STUDY; CHEMISTRY; DEFICIENCY; GENETICS; METABOLISM; MIDDLE AGED; PATHOLOGY;

CASE-CONTROL STUDIES; DNA PRIMERS; HUMANS; HYPOKALEMIA; HYPOKALEMIC PERIODIC PARALYSIS; KATP CHANNELS; MALE; MIDDLE AGED; MUSCLE, SKELETAL; POTASSIUM; POTASSIUM CHANNELS, INWARDLY RECTIFYING; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 67749096174     PISSN: 17528054     EISSN: 17528062     Source Type: Journal    
DOI: 10.1111/j.1752-8062.2008.00007.x     Document Type: Article

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