Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Kour S，Rajan DS，Fortuna TR，Anderson EN，Ward C，Lee Y，Lee S，闪亮的B，Chae JH，Choi M，Siquier K，Cantagrel V，Amiel J，Stolerman ES，Barnett SS，Cousin MA，Castro D，Castro D，McDonald K，Kirmse B，Nemeth AH，Rajasundaram D，Rajasundaram D，Innes AM，Lynch D，Frosk P，Frosk P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins P，Collins AM，CollinsA，Gibbons M，Yang M，Desguerre I，Boddaert N，Gitiaux C，Rydning SL，Selmer KK，Urreizti R，Garcia-Oguiza A，Osorio AN，Verdura A，Pujol A，Pujol A，Pujol A，McCurry A，McCurry HR，Landers Je，Landers Je，Agnihotri s，and andriescu s，and andriescuuEC, Moody SB, Phornphutkul C, Sacoto MJG, Begtrup A, Houlden H, Kirschner J, Schorling D, Rudnik-Schöneborn S, Strom TM, Leiz S, Juliette K, Richardson R, Yang Y, Zhang Y, Wang M, WangJ，Wang X，Platzer K，Donkervoort S，BönnemannCG，Wagner M，Issa MY，Elbendary HM，Stanley V，Maroofian R，Gleeson JG，Zaki JG，Zaki MS，Senderek J，Senderek J，Pandey UB。
Kour S, et al. Among authors:shin yb.
纳特社区。2021 May 7;12(1):2558. doi: 10.1038/s41467-021-22627-w.
纳特社区。2021。
PMID：33963192
Free PMC article.
