Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el gen SLC19A2:  caso clínico

doi:10.5546/aap.2017.e153

Arch Argent Pediat

2017

DOI: 10.5546/aap.2017.e153

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Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el gen SLC19A2: caso clínico

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Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el gen SLC19A2: caso clínico

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References 6 publications

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