Overview

Hers disease


Show Summary Details

Quick Reference

A hereditary glycogen storage disease in humans arising from a deficiency of the enzyme hepatic phosphorylase. It is inherited as an autosomal recessive trait with an incidence of 1/200,000.

Subjects: Genetics and Genomics.


Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.