Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa.


Aoyama Y., Endo Y., Ebara T., Murase T., Shin Y. S., Podskarbi T., ...Daha Fazla

Pediatrics international : official journal of the Japan Pediatric Society, cilt.52, sa.1, ss.145-7, 2010 (SCI-Expanded) identifier identifier identifier