Heterozygous TERT gene mutation associated with familial idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease of unknown cause that occurs sporadically, but it can also occur in families and so named as Familial Pulmonary Fibrosis (FPF). Some forms of FPF overlaps IPF features, namely the radiological and histological pattern of usua...

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Detalles Bibliográficos
Autores principales: Sousa, S.R., Caetano Mota, P., Melo, N., Bastos, H.N., Padrão, E., Pereira, J.M., Cunha, R., Souto Moura, C., Guimarães, S., Morais, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304384/
https://www.ncbi.nlm.nih.gov/pubmed/30603600
http://dx.doi.org/10.1016/j.rmcr.2018.12.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304384/
https://www.ncbi.nlm.nih.gov/pubmed/30603600
http://dx.doi.org/10.1016/j.rmcr.2018.12.005

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