Literature DB >> 11121156

Congenital erythropoietic porphyria: a novel homozygous mutation in a Japanese patient.

T Rogounovitch, N Takamura, I Hombrados, C Morel, T Tanaka, Y Kameyoshi, Y Shimizu-Yoshida, H de Verneuil, S Yamashita.   

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Year:  2000        PMID： 11121156     DOI： 10.1046/j.1523-1747.2000.0202a.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  2 in total

1.  Crystal structure of human uroporphyrinogen III synthase.

Authors:  M A Mathews; H L Schubert; F G Whitby; K J Alexander; K Schadick; H A Bergonia; J D Phillips; C P Hill
Journal:  EMBO J       Date:  2001-11-01       Impact factor: 11.598

2.  Mutational analysis of uroporphyrinogen III cosynthase gene in Iranian families with congenital erythropoietic porphyria.

Authors:  Meysam Moghbeli; Mahmood Maleknejad; Azadeh Arabi; Mohammad Reza Abbaszadegan
Journal:  Mol Biol Rep       Date:  2012-02-18       Impact factor: 2.316
  2 in total

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