HEP is an autosomal recessive disease caused by mutations in the gene responsible for PCT, the uroporphyrinogen decarboxylase gene (UROD), located at 1p34.
HEP results from a defect in uroporphyrinogen decarboxylase activity (step 5), and is caused by defects in the same gene as PCT.
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HEP is linked to a deficiency of uroporphyrinogen decarboxylase in both the liver and the bone marrow.
Hepatoerythopoietic porphyria (HEP) affects heme biosynthesis in both the liver and the bone marrow.
Hep B (hepatitis B vaccine)-Hep B is given as a series of three injections.
The majority of cases of "Hep C" are due to intravenous drug use.
HEP seems to be inherited in an autosomal recessive manner.
People with "Hep B" also experience vomiting.
This page gives an overview of all articles in the 1911 Brittanica which are alphabetized under Hep to Hes.