Congenital erythropoietic porphyria (Günther's disease): enzymatic studies on two cases of late onset. | J Lab Clin Med;97(4): 551-8, 1981 Apr. | MEDLINE

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Congenital erythropoietic porphyria (Günther's disease): enzymatic studies on two cases of late onset.

Deybach, J C; de Verneuil, H; Phung, N; Nordmann, Y; Puissant, A; Boffety, B.

J Lab Clin Med ; 97(4): 551-8, 1981 Apr.

Article in En | MEDLINE | ID: mdl-7205063

Subject(s)

Isomerases/metabolism; Photosensitivity Disorders/enzymology; Porphyrias/enzymology; Uroporphyrinogen III Synthetase/metabolism; Adult; Erythropoiesis; Humans; Male; Pedigree; Photosensitivity Disorders/congenital; Porphyrias/congenital; Time Factors

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Collection: 01-internacional Database: MEDLINE Main subject: Photosensitivity Disorders / Porphyrias / Uroporphyrinogen III Synthetase / Isomerases Limits: Adult / Humans / Male Language: En Journal: J Lab Clin Med Year: 1981 Document type: Article Country of publication: United States

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Collection: 01-internacional Database: MEDLINE Main subject: Photosensitivity Disorders / Porphyrias / Uroporphyrinogen III Synthetase / Isomerases Limits: Adult / Humans / Male Language: En Journal: J Lab Clin Med Year: 1981 Document type: Article Country of publication: United States