遺伝子テクノロジー

症例報告

Two Novel Mutations in the AGK Gene: Two Case Reports with Sengers Syndrome

• Deniz Kor, Berna Seker Yılmaz, Ozden Ozgur Horoz, Gulay Ceylaner, Selcuk Sızmaz, Fadli Demir and Neslihan Onenli Mungan

症例報告

Hereditary Xanthinuria with Recurrent Urolithiasis Occurring in Infancy

• Afef Bahlous, Mehdi M’rad, Eya Kalaie, Mouna Bouksila, Manef Gasmi, Amira Mohsni, Kahena Bouzid and Jaouida Abdelmoula

総説

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

• Khandrika L, Parsam V, Mahalingam M, Musmoori SG, Nandan U,Dange S, Sahoo PK, Rath PC and Jain J