Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations-Reference-Cited by-同舟云学术

Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations

Published:2009-11-24 Issue:4 Volume:19 Page:584-596
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Clavero Sonia,Bishop David F.,Haskins Mark E.,Giger Urs,Kauppinen Raili,Desnick Robert J.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/19/4/584/17250625/ddp525.pdf

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4. A novel stop codon mutation (X417L) of the ferrochelatase gene in bovine protoporphyria, a natural animal model of the human disease;Jenkins;Biochim. Biophys. Acta,1998

5. Congenital porphyria in pigs;Jorgensen;Br. Vet. J.,1959

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