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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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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3896844/ https://ncbi.nlm.nih.gov/pubmed/24438707 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1710-1492-10-2 |
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