Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

BMC Medical Genomics

Youssef Zghib¹  Hala Wannous¹  Hossam Murad²  Mohamad Baseel Alhalabi²  Amir Dabboul²  Nour Alfakseh²  Mohamad Sayah Nweder² 

[1] Chlidien’s Hospital of Damascus, Damascus, Syria;Human Genetics Division, Molecular Biology and Biotechnology Department, Human Genetics Division, Atomic Energy Commission of Syria, P.O. Box 6091, Damascus, Syria;

关键词: Primary hyperoxaluria type 1;    AGXT;    Syria;   

DOI  :  10.1186/s12920-021-00996-x

来源: Springer

【 授权许可】

CC BY