A different isoform of the transport protein mutated in the glycogen storage disease 1b is expressed in brain.

doi:10.1016/s0014-5793(98)00878-3

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Article

A different isoform of the transport protein mutated in the glycogen storage disease 1b is expressed in brain.

FEBS letters - 14 Aug 1998

Middleditch C, Clottes E, Burchell A

Abstract excerpt

There are differences in the kinetic properties of the liver and brain microsomal glucose-6-phosphate transport systems suggesting the possibility of tissue specific isoforms. The availability of a human liver cDNA sequence which is mutated in patients with deficiencies of liver microsomal glucos...

Topics

Amino Acid Sequence
Animals
Base Sequence
Blotting, Northern
Brain
Cloning, Molecular
Gene Expression
Glucose-6-Phosphatase
Glycogen Storage Disease Type I
Humans
Isoenzymes
Microsomes, Liver

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Molecular Sequence Data

Mutation

RNA, Messenger

Rats

Sequence Alignment

Sequence Analysis

Source

Open in PubMed

Identifiers

PMID: 9738927
DOI: 10.1016/s0014-5793(98)00878-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9738927-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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