Rare surfactant‐related variants in familial and sporadic pulmonary fibrosis

The role of constitutional genetic defects in idiopathic pulmonary fibrosis (IPF) is increasingly appreciated. Monogenic disorders associated with IPF affect two pathways: telomere maintenance, accounting for approximately 10% of all patients with IPF, and surfactant biology, responsible for 1%–3% o...

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Detalles Bibliográficos
Autores principales: Sutton, Rachel M., Bittar, Humberto Trejo, Sullivan, Daniel I., Silva, Agustin Gil, Bahudhanapati, Harinath, Parikh, Anishka H., Zhang, Yingze, Gibson, Kevin, McDyer, John F., Kass, Daniel J., Alder, Jonathan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771972/
https://www.ncbi.nlm.nih.gov/pubmed/36135709
http://dx.doi.org/10.1002/humu.24476

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771972/
https://www.ncbi.nlm.nih.gov/pubmed/36135709
http://dx.doi.org/10.1002/humu.24476

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