Genetic Variants for Long QT Syndrome among Infants and Children from a Statewide Newborn Hearing Screening Program Cohort-Reference-Cited by-同舟云学术

Genetic Variants for Long QT Syndrome among Infants and Children from a Statewide Newborn Hearing Screening Program Cohort

Published:2014-03 Issue:3 Volume:164 Page:590-595.e3
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Chang Ruey-Kang R.,Lan Yueh-Tze,Silka Michael J.,Morrow Hallie,Kwong Alan,Smith-Lang Janna,Wallerstein Robert,Lin Henry J.

Funder

Clinical and Translational Science Institute, University of California, Los Angeles

National Institutes of Health

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference32 articles.

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3. The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome;Schwartz;Circulation,2006

4. Congenital deafness associated with electrocardiographic abnormalities, fainting attacks and sudden death. a recessive syndrome;Fraser;Q J Med,1964

5. Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosity;Giudicessi;Circ Cardiovasc Genet,2013

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