国际标准期刊号: 2329-6682
案例报告
Two Novel Mutations in the AGK Gene: Two Case Reports with Sengers Syndrome
Hereditary Xanthinuria with Recurrent Urolithiasis Occurring in Infancy
评论文章
A Rapid Real-Time PCR Assay for CYP2C19 Gene Variants to Optimize the Use of Clopidogrel and Other Anti-Platelet Drugs for PCI Stent Patients