Gastrointestinal symptoms in families of patients with an SCN5A-encoded cardiac channelopathy: Evidence of an intestinal channelopathy

American Journal of Gastroenterology

Volumn 101, Issue 6, 2006, Pages 1299-1304

  Locke III, G Richard ^a,b   Ackerman, Michael J ^c   Zinsmeister, Alan R ^a,d   Thapa, Prabin ^d   Farrugia, Gianrico ^a,b,e  

^a Enteric Neuroscience Program   (United States)

^b Division of Gastroenterology and Hepatology   (United States)

^c Departments of Medicine Pediatrics and Molecular Pharmacology

^d Mayo Clinic   (United States)

^e MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL HERG; SODIUM CHANNEL; SODIUM CHANNEL AFFECTING AGENT;

ADOLESCENT; ADULT; AGED; ARTICLE; COILED BODY; COMPLEX FORMATION; FAMILIAL DISEASE; FEMALE; GASTROINTESTINAL SYMPTOM; GENE; GENETIC ANALYSIS; HIGH RISK PATIENT; HUMAN; LEYDIG CELL; LOGISTIC REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MALE; MULTIGENE FAMILY; MUTATIONAL ANALYSIS; PATHOGENESIS; PRIORITY JOURNAL; QT PROLONGATION; SCN5A GENE; SMOOTH MUSCLE FIBER; SYMPTOMATOLOGY;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GASTROINTESTINAL DISEASES; GENOTYPE; HUMANS; INFANT; KCNQ POTASSIUM CHANNELS; LOGISTIC MODELS; LONG QT SYNDROME; MALE; MIDDLE AGED; MUTATION; QUESTIONNAIRES; SODIUM CHANNELS;

EID: 33744794378     PISSN: 00029270     EISSN: 15720241     Source Type: Journal    
DOI: 10.1111/j.1572-0241.2006.00507.x     Document Type: Article

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