Cite
HARVARD Citation
Çıralı, C. et al. (n.d.). P385 Hypotonic infant with riboflavin transporter deficiency due to slc52a2 mutations. Archives of disease in childhood. pp. A181-A182. [Online].
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Çıralı, C. et al. (n.d.). P385 Hypotonic infant with riboflavin transporter deficiency due to slc52a2 mutations. Archives of disease in childhood. pp. A181-A182. [Online].