High prevalence of four long QT syndrome founder mutations in the Finnish population

AIMS: Long QT syndrome (LQTS) is an inherited arrhythmia disorder with an estimated prevalence of 0.01%–0.05%. In Finland, four founder mutations constitute up to 70% of the known genetic spectrum of LQTS. In the present survey, we sought to estimate the actual prevalence of the founder mutations an...

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Bibliografski detalji
Glavni autori: MARJAMAA, ANNUKKA, SALOMAA, VEIKKO, NEWTON-CHEH, CHRISTOPHER, PORTHAN, KIMMO, REUNANEN, ANTTI, KARANKO, HANNU, JULA, ANTTI, LAHERMO, PÄIVI, VÄÄNÄNEN, HEIKKI, TOIVONEN, LAURI, SWAN, HEIKKI, VIITASALO, MATTI, NIEMINEN, MARKKU S., PELTONEN, LEENA, OIKARINEN, LASSE, PALOTIE, AARNO, KONTULA, KIMMO
Format: Artigo
Jezik:Inglês
Izdano: 2009
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2704397/
https://ncbi.nlm.nih.gov/pubmed/19160088
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/07853890802668530
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