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Exome Sequencing Identifies Mutant TINF2 in a Family With Pulmonary Fibrosis
BACKGROUND: Short telomeres are a common defect in idiopathic pulmonary fibrosis, yet mutations in the telomerase genes account for only a subset of these cases. METHODS: We identified a family with pulmonary fibrosis, idiopathic infertility, and short telomeres. RESULTS: Exome sequencing of blood-d...
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| Publicado no: | Chest |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American College of Chest Physicians
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4420184/ https://ncbi.nlm.nih.gov/pubmed/25539146 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1378/chest.14-1947 |
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