Associated Papers
Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa.
Aoyama Y et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2010
Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.
Aoyama Y et al.
Journal of Human Genetics, 2009
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