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Structure and mutation analysis of the glycogen storage disease type 1b gene

✍ Scribed by Paola Marcolongo; Virginia Barone; Giuseppina Priori; Barbara Pirola; Sabrina Giglio; Giacomo Biasucci; Enrico Zammarchi; Giancarlo Parenti; Ann Burchell; Angelo Benedetti; Vincenzo Sorrentino


Book ID
117109767
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
74 KB
Volume
436
Category
Article
ISSN
0014-5793

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πŸ“œ SIMILAR VOLUMES


Glycogen storage disease type Ib: Struct
✍ Hou, Dian-Chang; Kure, Shigeo; Suzuki, Yoichi; Hasegawa, Yukihiro; Hara, Yoji; I πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 70 KB πŸ‘ 2 views

Glycogen storage disease type Ib is caused by a mutation in the gene encoding microsomal glucose-6-phosphate (G6P) transporter. We determined the exon/intron organization of the G6P transporter gene. Four overlapping genomic fragments containing the entire coding region of the gene were amplified by