Maternal riboflavin deficiency, resulting in transient neonatal‐onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B
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John J. Mitchell | J. Christodoulou | S. Masuda | A. Yonezawa | G. Peters | R. Olsen | K. Inui | G. Ho | K. Carpenter | W. Rhead | K. Sim