Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome
Pendred 综合征中 EPHA2 和 SLC26A4 突变的双基因遗传
期刊:Nature Communications
影响因子:14.7
doi:10.1038/s41467-020-15198-9
Mengnan Li, Shin-Ya Nishio, Chie Naruse, Meghan Riddell, Sabrina Sapski, Tatsuya Katsuno, Takao Hikita, Fatemeh Mizapourshafiyi, Fiona M Smith, Leanne T Cooper, Min Goo Lee, Masahide Asano, Thomas Boettger, Marcus Krueger, Astrid Wietelmann, Johannes Graumann, Bryan W Day, Andrew W Boyd, Stefan Offe
