Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ghada I.Z. Ali"'
Autor:
Magd A. Kotb, Lobna Mansour, Christine William Shaker Basanti, Wael El Garf, Ghada I.Z. Ali, Sally T. Mostafa El Sorogy, Inas E.M. Kamel, Naglaa M Kamal
Publikováno v:
Journal of Advanced Research, Vol 12, Iss , Pp 39-45 (2018)
Classic galactosemia is caused by deficiency of galactose-1-phosphate uridylyltransferase (GALT). It causes serious morbidity and mortality if left untreated. Screening for galactosemia is not included in Egyptian neonatal screening program. The stud
Externí odkaz:
https://doaj.org/article/54ed766f74b343e1aaaff8d98f8c036a
Autor:
Naglaa M. Kamal, Sally T. Mostafa El Sorogy, Ghada I.Z. Ali, Wael El Garf, Magd A. Kotb, Inas E.M. Kamel, Christine William Shaker Basanti, Lobna Mansour
Publikováno v:
Journal of Advanced Research, Vol 12, Iss, Pp 39-45 (2018)
Journal of Advanced Research
Journal of Advanced Research
Graphical abstract
Classic galactosemia is caused by deficiency of galactose-1-phosphate uridylyltransferase (GALT). It causes serious morbidity and mortality if left untreated. Screening for galactosemia is not included in Egyptian neonatal scr
Classic galactosemia is caused by deficiency of galactose-1-phosphate uridylyltransferase (GALT). It causes serious morbidity and mortality if left untreated. Screening for galactosemia is not included in Egyptian neonatal scr