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

dc.contributor.authorOzer, Isil
dc.contributor.authorEndo, Yoriko
dc.contributor.authorEbara, Tetsu
dc.contributor.authorMurase, Toshio
dc.contributor.authorShin, Yoon S.
dc.contributor.authorPodskarbi, Teodor
dc.contributor.authorOkubo, Minoru
dc.contributor.authorGoekcay, Gülden Fatma
dc.contributor.authorAoyama, Yoshiko
dc.contributor.authorDemirkol, Muebeccel
dc.date.accessioned2021-03-04T15:11:03Z
dc.date.available2021-03-04T15:11:03Z
dc.date.issued2010
dc.identifier.citationAoyama Y., Endo Y., Ebara T., Murase T., Shin Y. S. , Podskarbi T., Ozer I., Demirkol M., Goekcay G. F. , Okubo M., "Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa.", Pediatrics international : official journal of the Japan Pediatric Society, cilt.52, sa.1, ss.145-7, 2010
dc.identifier.issn1328-8067
dc.identifier.othervv_1032021
dc.identifier.otherav_856a132f-76f5-4303-873e-7ae3ffffed72
dc.identifier.urihttp://hdl.handle.net/20.500.12627/90721
dc.identifier.urihttps://doi.org/10.1111/j.1442-200x.2009.02943.x
dc.language.isoeng
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleNovel AGL mutation in a Turkish patient with glycogen storage disease type IIIa.
dc.typeMakale
dc.relation.journalPediatrics international : official journal of the Japan Pediatric Society
dc.contributor.department, ,
dc.identifier.volume52
dc.identifier.issue1
dc.identifier.startpage145
dc.identifier.endpage7
dc.contributor.firstauthorID195103


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