Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A

International Journal of Cardiology

Volumn 167, Issue 6, 2013, Pages 3078-3080

  Kodama, Takahide ^a   Serio, Alessandra ^a   Disertori, Marcello ^b   Bronzetti, Gabriele ^c   Diegoli, Marta ^a   Narula, Nupoor ^a   Grasso, Maurizia ^a   Mazzola, Silvia ^b   Arbustini, Eloisa ^a  

^a FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

^b SANTA CHIARA HOSPITAL   (Italy)

^c UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

Autosomal recessive; SCN5A gene; Sick sinus syndrome

Indexed keywords

DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; SODIUM CHANNEL NAV1.5;

AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CLINICAL EVALUATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; GENE; GENE MUTATION; GENETIC SCREENING; HOLTER MONITORING; HUMAN; IMPLANTED HEART PACEMAKER; LETTER; MALE; MEDICAL HISTORY; PATIENT MONITORING; PRESCHOOL CHILD; PRIORITY JOURNAL; SCN5A GENE; SICK SINUS SYNDROME;

AUTOSOMAL RECESSIVE; SCN5A GENE; SICK SINUS SYNDROME;

CHILD; FEMALE; HUMANS; MALE; MUTATION; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; PEDIGREE; SICK SINUS SYNDROME;

EID: 84883773991     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2012.11.062     Document Type: Article

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