YI-DER JIANGYI-CHENG CHANGChiu, Yen-FengYen-FengChiuTIEN-JYUN CHANGHUNG-YUAN LILin, Wen-HsingWen-HsingLinYuan, Hsiang-YuHsiang-YuYuanChen, Yuan-TsongYuan-TsongChenLEE-MING CHUANG2023-02-082023-02-082010-08-251471-2350https://scholars.lib.ntu.edu.tw/handle/123456789/627755Recent data indicate that loss-of-function mutation in the gene encoding the facilitative glucose transporter GLUT10 (SLC2A10) causes arterial tortuosity syndrome via upregulation of the TGF-β pathway in the arterial wall, a mechanism possibly causing vascular changes in diabetes.enTORTUOSITY-SYNDROME; VASCULAR-DISEASE; RISK-FACTORS; LOWER-EXTREMITY; COMPLICATIONS; POPULATION; ASSOCIATION; MUTATIONS; TRAITS[SDGs]SDG3SLC2A10 genetic polymorphism predicts development of peripheral arterial disease in patients with type 2 diabetes. SLC2A10 and PAD in type 2 diabetesjournal article10.1186/1471-2350-11-126207358552-s2.0-77955804588WOS:000283195100001https://api.elsevier.com/content/abstract/scopus_id/77955804588