Tags: Disease.

Enolase Deficiency is a rare genetic disorder of glucose metabolism. Partial deficiencies have been observed in several caucasian families. The deficiency is transmitted through an autosomal dominant inheritance pattern. The gene for Enolase 1 has been localized to Chromosome 1 in humans. Enolase deficiency like other glycolytic enzyme deficiences usually manifests in red blood cells as they rely entirely on anaerobic glycolysis.

Loading...

This page contains content from the copyrighted Wikipedia article "Enolase deficiency"; that content is used under the GNU Free Documentation License (GFDL). You may redistribute it, verbatim or modified, providing that you comply with the terms of the GFDL.