TY  - JOUR
AU  - Farre, Xavier
AU  - Espin, Roderic
AU  - Baiges, Alexandra
AU  - Blommaert, Eline
AU  - Kim, Wonji
AU  - Giannikou, Krinio
AU  - Herranz, Carmen
AU  - Roman, Antonio
AU  - Saez, Berta
AU  - Casanova, Alvaro
AU  - Ancochea, Julio
AU  - Valenzuela, Claudia
AU  - Ussetti, Piedad
AU  - Laporta, Rosalia
AU  - Rodriguez-Portal, Jose A
AU  - van Moorsel, Coline H M
AU  - van der Vis, Joanne J
AU  - Quanjel, Marian J R
AU  - Tena-Garitaonaindia, Mireia
AU  - Sanchez de Medina, Fermín
AU  - Mateo, Francesca
AU  - Molina-Molina, Maria
AU  - Won, Sungho
AU  - Kwiatkowski, David J
AU  - de Cid, Rafael
AU  - Pujana, Miquel Angel
PY  - 2021
DO  - 10.1183/23120541.00375-2021
SN  - 2312-0541
UR  - http://hdl.handle.net/10668/20258
T2  - ERJ open research
AB  - 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...
LA  - en
PB  - European Respiratory Society
KW  - Humans
KW  - Female
KW  - Forced Expiratory Volume
KW  - Genome-Wide Association Study
KW  - Transcriptome
KW  - Lymphangioleiomyomatosis
KW  - Genetic Pleiotropy
KW  - Lung
KW  - Vital Capacity
KW  - Spirometry
KW  - Genomics
KW  - Gene Expression Profiling
TI  - Evidence for shared genetic risk factors between lymphangioleiomyomatosis and pulmonary function.
TY  - research article
VL  - 8
ER  -