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...
Kaydedildi:
| Yazar: | |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
EDP Sciences
2026-01-01
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| Seri Bilgileri: | BIO Web of Conferences |
| Online Erişim: | https://www.bio-conferences.org/articles/bioconf/pdf/2026/43/bioconf_cebs2026_01002.pdf |
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