Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).

TitleGenetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).
Publication TypeJournal Article
AuthorsBramswig, NC, Bertoli-Avella, AM, Albrecht, B, Aqeel, AIAl, Alhashem, A, Al-Sannaa, N, Bah, M, Bröhl, K, Depienne, C, Dorison, N, Doummar, D, Ehmke, N, Elbendary, HM, Gorokhova, S, Héron, D, Horn, D, James, K, Keren, B, Kuechler, A, Ismail, S, Issa, MY, Marey, I, Mayer, M, McEvoy-Venneri, J, Megarbane, A, Mignot, C, Mohamed, S, Nava, C, Philip, N, Ravix, C, Rolfs, A, Sadek, AAbdrabou, Segebrecht, L, Stanley, V, Trautman, C, Valence, S, Villard, L, Wieland, T, Engels, H, Strom, TM, Zaki, MS, Gleeson, JG, Lüdecke, H-J, Bauer, P, Wieczorek, D
PubMed ID30167850
Grant List01GS08164 / / Bundesministerium für Bildung und Forschung /
01GS08167 / / Bundesministerium für Bildung und Forschung /
01GS08163 / / Bundesministerium für Bildung und Forschung /
U54HG003067 / / Broad Institute /
UM1HG008900 / / Broad Institute /
U54HG006504 / / Yale Center for Mendelian Disorders /
R01NS048453 / / National Institutes of Health /
R01NS052455 / / National Institutes of Health /