NPT4, a new microsomal phosphate transporter: Mutation analysis in glycogen storage disease type Ic-Reference-Cited by-同舟云学术

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NPT4, a new microsomal phosphate transporter: Mutation analysis in glycogen storage disease type Ic

Published:2004-11 Issue:6 Volume:27 Page:725-733
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Melis D.¹²,Havelaar A. C.¹,Verbeek E.¹,Smit G. P. A.³,Benedetti A.⁴,Mancini G. M. S.¹,Verheijen F.¹

Affiliation:

1. ; Department of Clinical Genetics; Erasmus University Rotterdam; The Netherlands

2. ; Department of Pediatrics; ‘Federico II’ University; Naples Italy

3. ; Beatrix Children's Hospital; University Hospital Groningen; The Netherlands

4. ; Institute of General Pathology; University of Sienna; Sienna Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/B:BOLI.0000045755.89308.2f/fullpdf

Reference19 articles.

1. Evidence for the participation o independent translocation or phosphate and glucose 6-phosphate in the microsomal glucose-6-phosphatase system. Interactions of the system with orthophosphate, inorganic pyrophosphate, and carbamyl phosphate;Arion;J Bol Chem,1980

2. Uptake of glutamate into synaptic vesicles by an inorganic phosphate transporter;Bellocchio;Science,2000

3. Molecular cloning of the cDNA encoding a human renal sodium phosphate transport protein and its assignment to chromo-some 6p21.3-p23;Chong;Genomics,1993

4. Mutations in the glucose 6-phosphate transporter (G6PT)gene in patients with glycogen storage diseases type 1b and 1c;Galli;FEBS Lett,1999

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