Glycometabolism and Fructose-1,6-bisphosphatase Deficiency Disease
Fructose-1,6-bisphosphatase (FBP) deficiency disease is a rare autosomal recessive inherited metabolic disorder. It has defects in key enzymes of the liver gluconeogenesis pathway caused by FBP1 gene mutation of Zone q22 in the chromosome 9#. Since FBP is the last step of rate-limiting enzyme of glu...
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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
EDP Sciences
2026-01-01
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| Edice: | BIO Web of Conferences |
| On-line přístup: | https://www.bio-conferences.org/articles/bioconf/pdf/2026/43/bioconf_cebs2026_01002.pdf |
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