Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

Journal of Clinical Investigation

Volumn 110, Issue 3, 2002, Pages 381-388

  Tristani Firouzi, Martin ^a   Jensen, Judy L ^a   Donaldson, Matthew R ^a   Sansone, Valeria ^b   Meola, Giovanni ^b   Hahn, Angelika ^c   Bendahhou, Said ^a   Kwiecinski, Hubert ^d   Fidzianska, Anna ^e   Plaster, Nikki ^a   Fu, Ying Hui ^f   Ptacek, Louis J ^a   Tawil, Rabi ^g  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MILAN   (Italy)

^c LONDON HEALTH SCIENCES CENTRE   (Canada)

^d MEDICAL UNIVERSITY OF WARSAW   (Poland)

^e POLISH ACADEMY OF SCIENCES   (Poland)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ANDERSEN SYNDROME; ARTICLE; BONE MALFORMATION; CLINICAL ARTICLE; FEMALE; GENE MUTATION; HEART ARRHYTHMIA; HEART MUSCLE CELL; HEART VENTRICLE ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MALE; NUCLEOTIDE SEQUENCE; PERIODIC PARALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0036324229     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI15183     Document Type: Article

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