TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci
TCF12单倍体不足导致常染色体显性遗传的卡尔曼综合征,并揭示了致病基因位点之间的网络级相互作用。
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddaa120
Erica E Davis,Ravikumar Balasubramanian,Zachary A Kupchinsky,David L Keefe,Lacey Plummer,Kamal Khan,Blazej Meczekalski,Karen E Heath,Vanesa Lopez-Gonzalez,Mary J Ballesta-Martinez,Gomathi Margabanthu,Susan Price,James Greening,Raja Brauner,Irene Valenzuela,Ivon Cusco,Paula Fernandez-Alvarez,Margaret E Wierman,Taibo Li,Kasper Lage,Priscila Sales Barroso,Yee-Ming Chan,William F Crowley,Nicholas Katsanis