Phosphoglycerate Mutase: Difference between revisions
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When phosphoglycerate mutase has a genetic defect, it results in a muscle disease that interferes with the processing of carbohydrates. The onset can occur anywhere from childhood to adulthood. The inheritance pattern is autosomal recessive. Symptoms include exercise intolerance, cramps, muscle pain, and permanent weakness. <ref>http://www.mda.org/disease/pgam.html</ref> | When phosphoglycerate mutase has a genetic defect, it results in a muscle disease that interferes with the processing of carbohydrates. The onset can occur anywhere from childhood to adulthood. The inheritance pattern is autosomal recessive. Symptoms include exercise intolerance, cramps, muscle pain, and permanent weakness. <ref>http://www.mda.org/disease/pgam.html</ref> | ||
==Additional Resources== | |||
For additional information, see: [[Carbohydrate Metabolism]] | |||
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==References== | |||
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