Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts
KCNJ10 或 FOXI1 突变与 Pendred 综合征/前庭导水管扩张的 SLC26A4 突变之间缺乏显著关联
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/1471-2350-14-85
Priya Landa, Ann-Marie Differ, Kaukab Rajput, Lucy Jenkins, Maria Bitner-Glindzicz