A hypotonic infant with methylene tetrahydrofolate reductase deficiency homozygous mutation of C 1015T G in MTFHR gene

SOYSAL Y. D., ÖZTÜRK M. N., HEKİM S. N.

The 4th Congress of theEuropean Academy of Pediatric Societies, 5 - 09 Ekim 2012

  • Yayın Türü: Bildiri
  • Marmara Üniversitesi Adresli: Evet