Telomere Shortening in Familial and Sporadic Pulmonary Fibrosis

Rationale: Heterozygous mutations in the coding regions of the telomerase genes, TERT and TERC, have been found in familial and sporadic cases of idiopathic interstitial pneumonia. All affected patients with mutations have short telomeres. Objectives: To test whether telomere shortening is a frequen...

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Bibliografiske detaljer
Main Authors: Cronkhite, Jennifer T., Xing, Chao, Raghu, Ganesh, Chin, Kelly M., Torres, Fernando, Rosenblatt, Randall L., Garcia, Christine Kim
Format: Artigo
Sprog:Inglês
Udgivet: American Thoracic Society 2008
Fag:
E. Interstitial Lung Disease
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2556455/
https://ncbi.nlm.nih.gov/pubmed/18635888
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200804-550OC
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