TRMA syndrome with a severe phenotype, cerebral infarction,...

BMC Pediatrics 2019 / 12 Vol. 19; Iss. 1

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, Xiumin
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Volume:
19
Journal:
BMC Pediatrics
DOI:
10.1186/s12887-019-1608-2
Date:
December, 2019
File:
PDF, 1.28 MB
2019
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