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,...

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Bibliografski detalji
Glavni autori: Chang, Ruey-Kang R., Lan, Yueh-Tze, Silka, Michael J., Morrow, Hallie, Kwong, Alan, Smith-Lang, Janna, Wallerstein, Robert, Lin, Henry J.
Format: Artigo
Jezik:Inglês
Izdano: 2013
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Article
Online pristup: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
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