Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-0960.2011.00875.x/fullpdf
Reference14 articles.
1. Characterisation 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. Porphyria in Switzerland, 15;Schneider-Yin;Swiss Med. Wkly,2009
3. Two novel mutations and coexistence of the 9991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporhyria;Wiman;J. Hum. Genet.,2002
4. Online Mendelian Inheritance in Man 2010 http://omim.org/entry/612732
5. Molecular mechanisms of dominant expression in porphyria;Badminton;J. Inherit. Metab. Dis.,2005
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