Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort

OBJECTIVES: Autosomal recessive long QT syndrome (LQTS), or Jervell and Lange-Nielsen syndrome (JLNS), can be associated with sensorineural hearing loss (SNHL). We aimed to explore newborn hearing screening combined with ECGs for early JLNS detection. STUDY DESIGN: We conducted California statewide,...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Chang, Ruey-Kang R., Lan, Yueh-Tze, Silka, Michael J., Morrow, Hallie, Kwong, Alan, Smith-Lang, Janna, Wallerstein, Robert, Lin, Henry J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3943925/
https://ncbi.nlm.nih.gov/pubmed/24388587
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpeds.2013.11.011
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados