학술논문
A disorder clinically resembling cystic fibrosis caused by biallelic variants in the AGR2 gene
Document Type
Article
Author
Bertoli-Avella, A.; Hotakainen, R.; Urzi, A.; Pareira, C.; Marais, A.; Morales-Torres, G.; Fisher, S.; Demuth, L.; Karageorgou, V.; Khan, S.; Hajjari, Z.; Radefeldt, M.; Al-Ali, R.; Tripolszki, K.; Jamhawi, A.; Paknia, O.; Cozma, C.; Ameziane, N.; Bauer, P.; Shehhi, M.A.; Aloraimi, S.; Shidhani, K.A.; Moteleb Selim, L.A.; Menabawy, N.A.; Busehail, M.; AlShaikh, M.; Gilani, N.; Chalabi, D.N.; Alharbi, N.S.; Alfadhel, M.; Abdelrahman, M.; Al-Muhsen, S.; Venselaar, H.; Anjum, N.; Saeed, A.; Cheema, H.; Alghamdi, M.A.; Aljaedi, H.; Arabi, H.
Source
In: Journal of Medical Genetics . (Journal of Medical Genetics, 2022, 59(10):993-1001)
Subject
Language
English
ISSN
14686244
00222593
00222593