Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Bell's Palsy[original query] |
---|
Chondroitin beta-1,4-N-acetylgalactosaminyltransferase-1 missense mutations are associated with neuropathies. Journal of human genetics 2010 Dec . Saigoh K, Izumikawa T, Koike T, Shimizu J, Kitagawa H, Kusunoki S |
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.
Scientific reports 2021 Feb 11 (1): 4188. Skuladottir Astros Th, Bjornsdottir Gyda, Thorleifsson Gudmar, Walters G Bragi, Nawaz Muhammad Sulaman, Moore Kristjan Helgi Swerford, Olason Pall I, Thorgeirsson Thorgeir E, Sigurpalsdottir Brynja, Sveinbjornsson Gardar, Eggertsson Hannes P, Magnusson Sigurdur H, Oddsson Asmundur, Bjornsdottir Anna, Vikingsson Arnor, Sveinsson Olafur A, Hrafnsdottir Maria G, Sigurdardottir Gudrun R, Halldorsson Bjarni V, Hansen Thomas Folkmann, Paarup Helene, Erikstrup Christian, Nielsen Kaspar, Klokker Mads, Bruun Mie Topholm, Sorensen Erik, Banasik Karina, Burgdorf Kristoffer S, Pedersen Ole Birger, Ullum Henrik, Jonsdottir Ingileif, Stefansson Hreinn, Stefansson Ka |
Genetic association of hypertension and several other metabolic disorders with Bell's palsy. Frontiers in genetics 2023 8 14 1077438. Huawei Liu, Qingyan Sun, Wenting Bi, Xiaodan Mu, Yongfeng Li, Min |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 13, 2024
- Content source: