Literature DB >> 6143037

Harderoporphyrin coproporphyria.

M Doss, R von Tiepermann, W Köpp.   

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Year:  1984        PMID： 6143037     DOI： 10.1016/s0140-6736(84)90169-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Coexistent hereditary coproporphyria and congenital erythropoietic porphyria (Günther disease).

Authors:  Y Nordmann; D Amram; J C Deybach; L N Phung; D Lesbros
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 2.  Hepatic porphyrias in children.

Authors:  G H Elder
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982

3.  Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.

Authors:  Alev Hasanoglu; Manisha Balwani; Ciğdem S Kasapkara; Fatih S Ezgü; Ilyas Okur; Leyla Tümer; Alpay Cakmak; Irina Nazarenko; Chunli Yu; Sonia Clavero; David F Bishop; Robert J Desnick
Journal:  J Inherit Metab Dis       Date:  2010-11-20       Impact factor: 4.982
  3 in total

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