Subclinical Lung Disease, Macrocytosis, and Premature Graying in Kindreds With Telomerase (TERT) Mutations

BACKGROUND: Mutations in the human gene encoding the protein component of telomerase (TERT) are the most common genetic defect in patients with familial idiopathic pulmonary fibrosis (IPF). The subclinical phenotypes of asymptomatic members of these families have not been evaluated with respect to T...

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Autori principali: Diaz de Leon, Alberto, Cronkhite, Jennifer T., Yilmaz, Cuneyt, Brewington, Cecelia, Wang, Richard, Xing, Chao, Hsia, Connie C. W., Garcia, Christine Kim
Natura: Artigo
Lingua:Inglês
Pubblicazione: American College of Chest Physicians 2011
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Original Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3168855/
https://ncbi.nlm.nih.gov/pubmed/21349926
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1378/chest.10-2865
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