T cell unresponsiveness in a pediatric cystic fibrosis patient: a case report

A girl was diagnosed with cystic fibrosis (CF) at birth, with repeatedly positive sweat tests and homozygous F508del mutations of her CF transmembrane conductance regulator (CFTR) gene. From an early age, her lung disease was more severe than her birth cohort peers despite aggressive treatment. At t...

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Detalles Bibliográficos
Autores principales: Kushwah, Rahul, Gagnon, Stéphane, Sweezey, Neil B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896844/
https://www.ncbi.nlm.nih.gov/pubmed/24438707
http://dx.doi.org/10.1186/1710-1492-10-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896844/
https://www.ncbi.nlm.nih.gov/pubmed/24438707
http://dx.doi.org/10.1186/1710-1492-10-2

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