BALB.NCT-Cpox is a unique mouse model of hereditary coproporphyria-Reference-Cited by-同舟云学术

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BALB.NCT-Cpox is a unique mouse model of hereditary coproporphyria

Published:2023-06 Issue: Volume:35 Page:100964
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Kang Xiaojing,Shimada Shin,Miyahara Hiroki,Higuchi Keiichi,Mori Masayuki

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Science and Technology Agency

Shinshu University

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference41 articles.

1. Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria;Lamoril;Am. J. Hum. Genet.,2001

2. Acute hepatic porphyria;Bissell;J. Clin. Transl. Hepatol.,2015

3. Haem arginate in acute hereditary coproporphyria;Manning;Arch. Dis. Child.,1991

4. Haem arginate as effective maintenance therapy for hereditary coproporphyria;Ma;Australas J. Dermatol.,2011

5. A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp);Lambie;Ann. Clin. Biochem.,2018

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