Associated Papers
Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease.
Chou JY et al.
Human Mutation, 2008
Structure-function analysis of human glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a.
Lei KJ et al.
The Journal of Biological Chemistry, 1995
[Case of a combination of enzyme-deficient forms of methemoglobinemia with enzyme-deficient hemolytic disease and reduced oxygenation of hemoglobin].
Gembitskiĭ EV et al.
Problemy Gematologii I Perelivaniia Krovi, 1975
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