家系全外显子组测序鉴定Wolfram综合征致病突变及其临床性状分析
孟祥雨, 闫丹丹, 陈香慧, 赖思宇, 徐云, 耿瑞娜, 张红, 张蓉, 胡承, 严婧

Identification of pathogenic mutations for a Wolfram syndrome pedigree by whole exome sequencing and analysis of its clinical characteristics
MENG Xiangyu, YAN Dandan, CHEN Xianghui, LAI Siyu, XU Yun, GENG Ruina, ZHANG Hong, ZHANG Rong, HU Cheng, YAN Jing
表1 测序引物序列
Tab 1 Sequences of the primers
Target mutationForward primer (5′→3′)Reverse primer (5′→3′)
R558HTTGGCCAGACCTTCATCACCCTCCAGAGACGTGAACCACC
S411Cfs*131GAGAACTTCCGCACCCTCACCTGACGTTGAGGACGACCAG