![](/img/cover-not-exists.png)
TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case report
Li, Xin, Cheng, Qing, Ding, Yu, Li, Qun, Yao, Ruen, Wang, Jian, Wang, XiuminVolume:
19
Language:
english
Journal:
BMC Pediatrics
DOI:
10.1186/s12887-019-1608-2
Date:
December, 2019
File:
PDF, 1.28 MB
english, 2019