Hereditary coproporphyria: incidence in a large English family.

Author:

Andrews J,Erdjument H,Nicholson D C

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Simultaneous excretion of coproporphyrin I and III in a case;Dobriner, K.

2. Watson C, Schwartz S, Schulze W, Jacobson L, Zagaria R. Studies in coproporphyrin III. J Clin Invest 1949;28: 465-8.

3. Hereditary coproporphyria. Study of a Swedish family;Haeger-Aronsen, B.; Stathers, G.; Swahn, G.;Ann Intern Med,1968

4. Dean G. Kramer S. Coproporphyria. S Afr Med J 1969; 43:138-42.

5. Hereditary coproporphyria. A family with unusually few and mild symptoms;Lomholt, J.C.; With, T.K.;Acta Med Scand

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2. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

3. Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria;The American Journal of Human Genetics;2001-05

4. Biochemical differentiation of the porphyrias;Clinical Biochemistry;1999-11

5. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999

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