Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
Arch Cardiovasc Dis
; 106(12): 635-43, 2013 Dec.
Article
em En
| MEDLINE
| ID: mdl-24140416
Palavras-chave
Alternative splicing; Brugada syndrome; Canal sodique cardiaque humain Na(v)1.5; Cardiac sodium channel Na(v)1.5; DM1; DMPK; DNA; Dystrophie myotonique de type 1; ECG; Human; Myotonic dystrophy type 1; PCR; RNA; RT; SCN5A; SD; Syndrome de Brugada; cDNA; complementary deoxyribonucleic acid; deoxyribonucleic acid; dystrophia myotonica protein kinase; dystrophia myotonica type 1; electrocardiogram; mRNA; messenger ribonucleic acid; polymerase chain reaction; reverse transcriptase; ribonucleic acid; standard deviation; Épissage alternatif
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Morte Súbita Cardíaca
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Processamento Alternativo
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Síndrome de Brugada
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Canal de Sódio Disparado por Voltagem NAV1.5
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Distrofia Miotônica
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article