A Hypotonic Infant with Fatal Methylenetetrahydrofolate Reductase Deficiency Due to Homozygote c 1015T G Mutation


Yalındağ Ozturk M. N., SOYSAL Y. D., HEKİM S. N., Türkdoğan D., ÖZTÜRK M. N.

Turkish Journal of Pediatric Emergency and Intensive Care Medicine, cilt.1, ss.43-48, 2014 (Hakemli Dergi)