Appropriateness of Newborn Screening for α1-Antitrypsin Deficiency

OBJECTIVE: The Alpha-1 Foundation convened a workshop to consider the appropriateness of newborn screening for α-1-antitrypsin (AAT) deficiency. METHODS: A review of natural history and technical data was conducted. RESULTS: Homozygous ZZ AAT deficiency is a common genetic disease occurring in 1 in...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Teckman, Jeffrey, Pardee, Erin, Howell, R. Rodney, Mannino, David, Sharp, Richard R., Brantly, Mark, Wanner, Adam, Lamson, Jamie
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2014
Assuntos:
Original Articles: Hepatology and Nutrition
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3901803/
https://ncbi.nlm.nih.gov/pubmed/24121147
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MPG.0000000000000196
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados