摘要
Objective To analyze and identify the mutations in SGLT2 gene of nine Chinese families with FRG,and determine the renal threshold for glucose excretion (RTG),so as to explore the association of genotype and RTG.Methods All coding regions of SGLT2 gene,including intron exon boundaries,were analyzed using PCR followed by direct sequence analysis.
作者
WANG Sai
望赛(Dept Nephrol,Affil Hosp,Qingdao Univ)