APA (7th ed.) Citation

Xin Li, Qing Cheng, Yu Ding, Qun Li, Ruen Yao, Jian Wang, & Xiumin Wang. (2019). TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: A case report. BMC.

Chicago Style (17th ed.) Citation

Xin Li, Qing Cheng, Yu Ding, Qun Li, Ruen Yao, Jian Wang, and Xiumin Wang. TRMA Syndrome with a Severe Phenotype, Cerebral Infarction, and Novel Compound Heterozygous SLC19A2 Mutation: A Case Report. BMC, 2019.

MLA (9th ed.) Citation

Xin Li, et al. TRMA Syndrome with a Severe Phenotype, Cerebral Infarction, and Novel Compound Heterozygous SLC19A2 Mutation: A Case Report. BMC, 2019.