Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q.

Author:

Fenske C D,Jeffery S,Weber J L,Houlston R S,Leonard J V,Lee P J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference19 articles.

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2. Evidence for changes in the conformational status of rat liver microsomal glucose6-phosphate:phosphohydrolase during detergentdependent membrane modification;Schulze, H.U.; Nolte, B.; Kannler, R.;Biol Chem,1986

3. Glycogen storage diseases;Chen, Y.T.; Burchell, A.,1995

4. The hepatic glycogen storage diseases problems beyond childhood;Lee, P.J.; Leonard, J.V.;Inherit Metab Dis,1995

5. Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type la;Lei, K.J.; Shelly, L.L.; Pan, C.J.; Sidbury, J.B.; Chou, J.Y.;Science,1993

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1. The sugar phosphate/phosphate exchanger family SLC37;Wiley Interdisciplinary Reviews: Membrane Transport and Signaling;2013-10-23

2. Glycogenosis type I – Von Gierke disease;Atlas of Inherited Metabolic Diseases 3E;2011-12-30

3. Glycogen Storage Disease: Clinical, Biochemical, and Molecular Heterogeneity;Seminars in Pediatric Neurology;2006-06

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5. The glucose-6-phosphatase system;BIOCHEM J;2002

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