Lung function in Birt-Hogg-Dub é syndrome: a retrospective analysis of 96 patients

Birt-Hogg-Dub é syndrome (BHD) is a rare autosomal dominant disorder caused by mutations in the FLCN gene coding for folliculin. Its clinical expression includes cutaneous fibrofolliculomas, renal tumors, multiple...

Source: Orphanet Journal of Rare Diseases - May 24, 2020 Category: Internal Medicine Authors: C. Daccord, V. Cottin, G. Pr évot, Y. Uzunhan, J. F. Mornex, P. Bonniaud, R. Borie, A. Briault, M. A. Collonge-Rame, B. Crestani, G. Devouassoux, O. Freynet, A. Gondouin, P. A. Hauss, C. Khouatra, S. Leroy & hellip; Tags: Research Source Type: research