TINF2 Gene Mutation in a Patient with Pulmonary Fibrosis

Pulmonary fibrosis is a frequent manifestation of telomere syndromes. Telomere gene mutations are found in up to 25% and 3% of patients with familial disease and sporadic disease, respectively. The telomere gene TINF2 encodes an eponymous protein that is part of the shelterin complex, a complex invo...

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Detalles Bibliográficos
Autores principales: Hoffman, T. W., van der Vis, J. J., van Oosterhout, M. F. M., van Es, H. W., van Kessel, D. A., Grutters, J. C., van Moorsel, C. H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818801/
https://www.ncbi.nlm.nih.gov/pubmed/27088026
http://dx.doi.org/10.1155/2016/1310862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818801/
https://www.ncbi.nlm.nih.gov/pubmed/27088026
http://dx.doi.org/10.1155/2016/1310862

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