Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.
Katipoğlu N, Karapinar TH, Demir K, Aydin Köker S, Nalbantoğlu Ö, Ay Y, Korkmaz HA, Oymak Y, Yıldız M, Tunç S, Hazan F, Vergin C, Ozkan B.
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Arch Argent Pediatr. 2017 Jun 1;115(3):e153-e156. doi: 10.5546/aap.2017.eng.e153.
Arch Argent Pediatr. 2017.
PMID: 28504500
Free article.
English, Spanish.