Literature DB >> 1208916

[Hereditary coproporphyria. Contribution of a case].

F Morell, J C Frisón, C Richart, I Martínez-Ballarín, C Llaras, J Almeida, A Caralps.   

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Year:  1975        PMID： 1208916

Source DB:  PubMed          Journal:  Rev Clin Esp        ISSN： 0014-2565            Impact factor:   1.556


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  1 in total

1.  Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia.

Authors:  Félix Javier Jiménez-Jiménez; José A G Agúndez; Carmen Martínez; Francisco Navacerrada; José Francisco Plaza-Nieto; Belén Pilo-de-la-Fuente; Hortensia Alonso-Navarro; Elena García-Martín
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2013-07-25
  1 in total

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