Functional analysis of mutations in the glucose-6-phosphate transporter that cause glycogen storage disease type Ib

The glucose-6-phosphate transporter (G6PT) deficient in glycogen storage disease type Ib is a phosphate (P(i))-linked antiporter capable of G6P:P(i) and P(i):P(i) exchanges. We previously characterized G6PT mutations by measuring G6P uptake activities in microsomes co-expressing G6PT and glucose-6-p...

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Détails bibliographiques
Auteurs principaux: Chen, Shih-Yin, Pan, Chi-Jiunn, Lee, Soojung, Peng, Wentao, Chou, Janice Y.
Format: Artigo
Langue:Inglês
Publié: 2008
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3422630/
https://ncbi.nlm.nih.gov/pubmed/18835800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2008.08.005
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