Heterozygous Cystic Fibrosis Transmembrane Regulator Gene Missense Variants Are Associated With Worse Cardiac Function in Patients With Duchenne Muscular Dystrophy.
Journal Of The American Heart Association
Jiang, Xuan X; Shao, Yanqiu Y; Araj, Faris G FG; Amin, Alpesh A AA; Greenberg, Benjamin M BM; Drazner, Mark H MH; Xing, Chao C; Mammen, Pradeep P A PPA
Publication Date: 2020-10-20
Variant appearance in text: ACSF3: Arg471Trp; rs138680796
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting.
American Journal Of Human Genetics
Wright, Caroline F CF; West, Ben B; Tuke, Marcus M; Jones, Samuel E SE; Patel, Kashyap K; Laver, Thomas W TW; Beaumont, Robin N RN; Tyrrell, Jessica J; Wood, Andrew R AR; Frayling, Timothy M TM; Hattersley, Andrew T AT; Weedon, Michael N MN
Publication Date: 2019-02-07
Variant appearance in text: ACSF3: R471W; rs138680796
Genomic and Transcriptomic Characterization Links Cell Lines with Aggressive Head and Neck Cancers.
Cell Reports
Cheng, Hui H; Yang, Xinping X; Si, Han H; Saleh, Anthony D AD; Xiao, Wenming W; Coupar, Jamie J; Gollin, Susanne M SM; Ferris, Robert L RL; Issaeva, Natalia N; Yarbrough, Wendell G WG; Prince, Mark E ME; Carey, Thomas E TE; Van Waes, Carter C; Chen, Zhong Z
Publication Date: 2018-10-30
Variant appearance in text: ACSF3: R471W; rs138680796
A Landscape of Pharmacogenomic Interactions in Cancer.
Cell
Iorio, Francesco F; Knijnenburg, Theo A TA; Vis, Daniel J DJ; Bignell, Graham R GR; Menden, Michael P MP; Schubert, Michael M; Aben, Nanne N; Gonçalves, Emanuel E; Barthorpe, Syd S; Lightfoot, Howard H; Cokelaer, Thomas T; Greninger, Patricia P; van Dyk, Ewald E; Chang, Han H; de Silva, Heshani H; Heyn, Holger H; Deng, Xianming X; Egan, Regina K RK; Liu, Qingsong Q; Mironenko, Tatiana T; Mitropoulos, Xeni X; Richardson, Laura L; Wang, Jinhua J; Zhang, Tinghu T; Moran, Sebastian S; Sayols, Sergi S; Soleimani, Maryam M; Tamborero, David D; Lopez-Bigas, Nuria N; Ross-Macdonald, Petra P; Esteller, Manel M; Gray, Nathanael S NS; Haber, Daniel A DA; Stratton, Michael R MR; Benes, Cyril H CH; Wessels, Lodewyk F A LFA; Saez-Rodriguez, Julio J; McDermott, Ultan U; Garnett, Mathew J MJ
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria.
Nature Genetics
Sloan, Jennifer L JL; Johnston, Jennifer J JJ; Manoli, Irini I; Chandler, Randy J RJ; Krause, Caitlin C; Carrillo-Carrasco, Nuria N; Chandrasekaran, Suma D SD; Sysol, Justin R JR; O'Brien, Kevin K; Hauser, Natalie S NS; Sapp, Julie C JC; Dorward, Heidi M HM; Huizing, Marjan M; , ; Barshop, Bruce A BA; Berry, Susan A SA; James, Philip M PM; Champaigne, Neena L NL; de Lonlay, Pascale P; Valayannopoulos, Vassilli V; Geschwind, Michael D MD; Gavrilov, Dimitar K DK; Nyhan, William L WL; Biesecker, Leslie G LG; Venditti, Charles P CP
Publication Date: 2011-08-14
Variant appearance in text: ACSF3: 1411C>T; Arg471Trp