TY  - GEN
AU  - Katipoğlu,Nagehan
AU  - Karapinar,Tuba H
AU  - Demir,Korean
AU  - Aydin Köker,Sultan
AU  - Nalbantoğlu,Özlem
AU  - Ay,Yılmaz
AU  - Korkmaz,Hüseyin A
AU  - Oymak,Yeşim
AU  - Yıldız,Melek
AU  - Tunç,Selma
AU  - Hazan,Filiz
AU  - Vergin,Canan
AU  - Ozkan,Behzat
TI  - Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report
SN  - 1668-3501
PY  - 2018///0511
KW  - Anemia, Megaloblastic
KW  - genetics
KW  - Diabetes Mellitus
KW  - Female
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Infant
KW  - Membrane Transport Proteins
KW  - Mutation
KW  - Thiamine Deficiency
KW  - congenital
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.5546/aap.2017.eng.e153
ER  -