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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

✍ Scribed by Aoyama, Yoshiko; Ozer, Isil; Demirkol, Mubeccel; Ebara, Tetsu; Murase, Toshio; Podskarbi, Teodor; Shin, Yoon S; Gokcay, Gulden; Okubo, Minoru


Book ID
121507060
Publisher
Nature Publishing Group
Year
2009
Tongue
English
Weight
324 KB
Volume
54
Category
Article
ISSN
1435-232X

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