Variants of human CLDN9 cause mild to profound hearing loss
人类CLDN9基因变异会导致轻度至重度听力损失。
期刊:Human Mutation
影响因子:3.3
doi:10.1002/humu.24260
Memoona Ramzan,Christophe Philippe,Inna A Belyantseva,Yoko Nakano,Cristina Fenollar-Ferrer,Risa Tona,Rizwan Yousaf,Rasheeda Basheer,Ayesha Imtiaz,Rabia Faridi,Zunaira Munir,Hafiza Idrees,Midhat Salman,Sophie Nambot,Antonio Vitobello,Souad Kartti,Oumaima Zarrik,P Dane Witmer,Nara Sobreria,Azeddine Ibrahimi,Botond Banfi,Sebastien Moutton,Thomas B Friedman,Sadaf Naz