Molecular Defects of Uroporphyrinogen Decarboxylase in a Patient with Mild Hepatoerythropoietic Porphyria-Reference-Cited by-同舟云学术

Molecular Defects of Uroporphyrinogen Decarboxylase in a Patient with Mild Hepatoerythropoietic Porphyria

Published:1994-05 Issue:5 Volume:102 Page:681-685
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Meguro Kuniaki,Fujita Hiroyoshi,Ishida Nobuhiro,Akagi Reiko,Kurihara Tatsuya,Galbraith Richard A,Kappas Attallah,Zabriskie John B,Sassa Shigeru,Toback Arnold C,Harber Leonard C

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference35 articles.

1. Purification and properties of uroporphyrinogen decarboxylase from human erythrocytes. A single enzyme catalyzing the four sequential decarboxy lations of uroporphyrinogens I and III;de Verneuil;J Biol Chem,1983

2. The Porphyrias, The Metabolic Basis of Inherited Disease;Kappas,1989

3. Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda?;Elder;Lancet,1981

4. Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family;Lazaro;Br J Dermatol,1984

5. Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria;de Verneuil;Am J Hum Genet,1984

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