Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report
NEK10 纯合截断突变与原发性纤毛运动障碍相关:病例报告
期刊:BMC Pulmonary Medicine
影响因子:2.8
doi:10.1186/s12890-020-1175-1
Al Mutairi, Fuad; Alkhalaf, Randa; Alkhorayyef, Abdullah; Alroqi, Fayhan; Yusra, Alyafee; Umair, Muhammad; Nouf, Fetaini; Khan, Amjad; Meshael, Alharbi; Hamad, Aleidi; Monira, Alaujan; Asiri, Abdulaziz; Alhamoudi, Kheloud M; Alfadhel, Majid