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PMID: 10911008 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

A molecular link between the sudden infant death syndrome and the long-QT syndrome.

The New England journal of medicine ·Vol. 343 ·No. 4 ·2000-07-27 ·Pages 262-7

Schwartz PJ, Priori SG, Dumaine R, Napolitano C, Antzelevitch C, Stramba-Badiale M, Richard TA, Berti MR, Bloise R

Abstract

暂无摘要

MeSH Terms
DNA Mutational Analysis Electrocardiography Gene Expression Humans Infant Long QT Syndrome/complications,diagnosis,genetics Male Mutation Polymorphism, Single-Stranded Conformational Sudden Infant Death/etiology
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Schwartz P J
Department of Cardiology, University of Pavia and Policlinico San Matteo Istituto di Ricovero e Cura a Carattere Scientifico, Italy. pjqt@compuserve.com
Priori S G
Dumaine R
Napolitano C
Antzelevitch C
Stramba-Badiale M
Richard T A
Berti M R
Bloise R
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
DOI
10.1056/NEJM200007273430405
Email
pjqt@compuserve.com
Published
2000-07-27
Pages
262-7
Language
English
Region
United States
NLM ID
0255562
Subset
IM
External Links
PubMed source DOI: 10.1056/NEJM200007273430405 View journal details
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