Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria

Subjects

Subjects :

Gene mutations -- Analysis
British -- Genetic aspects
Clinical enzymology -- Research
Biological sciences

Details

ISSN :

00029297

Volume :

68

Issue :

5

Database :

Gale General OneFile

Journal :

American Journal of Human Genetics

Publication Type :

Academic Journal

Accession number :

edsgcl.75247131