Evidence for shared genetic risk factors between lymphangioleiomyomatosis and pulmonary function

INTRODUCTION: Lymphangioleiomyomatosis (LAM) is a rare low-grade metastasising disease characterised by cystic lung destruction. The genetic basis of LAM remains incompletely determined, and the disease cell-of-origin is uncertain. We analysed the possibility of a shared genetic basis between LAM an...

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Detalles Bibliográficos
Autores principales: Farré, Xavier, Espín, Roderic, Baiges, Alexandra, Blommaert, Eline, Kim, Wonji, Giannikou, Krinio, Herranz, Carmen, Román, Antonio, Sáez, Berta, Casanova, Álvaro, Ancochea, Julio, Valenzuela, Claudia, Ussetti, Piedad, Laporta, Rosalía, Rodríguez-Portal, José A., van Moorsel, Coline H.M., van der Vis, Joanne J., Quanjel, Marian J.R., Tena-Garitaonaindia, Mireia, Sánchez de Medina, Fermín, Mateo, Francesca, Molina-Molina, María, Won, Sungho, Kwiatkowski, David J., de Cid, Rafael, Pujana, Miquel Angel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2022
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784893/
https://www.ncbi.nlm.nih.gov/pubmed/35083324
http://dx.doi.org/10.1183/23120541.00375-2021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784893/
https://www.ncbi.nlm.nih.gov/pubmed/35083324
http://dx.doi.org/10.1183/23120541.00375-2021

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