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

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

Open Access
|Jul 2013

Authors

Félix Javier Jiménez-Jiménez

fjavier.jimenez@salud.madrid.org

Section of Neurology, Hospital Universitario del Sureste, Arganda del Rey, Madrid

José A. G. Agúndez

info@ubiquitypress.com

Department of Pharmacology, University of Extremadura, Cáceres

Carmen Martínez

info@ubiquitypress.com

Department of Pharmacology, University of Extremadura, Cáceres

Francisco Navacerrada

info@ubiquitypress.com

Section of Neurology, Hospital Universitario del Sureste, Arganda del Rey, Madrid

José Francisco Plaza-Nieto

info@ubiquitypress.com

Section of Neurology, Hospital Universitario del Sureste, Arganda del Rey, Madrid

Belén Pilo-de-la-Fuente

info@ubiquitypress.com

Section of Neurology, Hospital Universitario del Sureste, Arganda del Rey, Madrid

Hortensia Alonso-Navarro

info@ubiquitypress.com

Section of Neurology, Hospital Universitario del Sureste, Arganda del Rey, Madrid

Elena García-Martín

info@ubiquitypress.com

Department of Biochemistry and Molecular Biology, University of Extremadura, Cáceres
DOI: https://doi.org/10.5334/tohm.145 | Journal eISSN: 2160-8288
Language: English
Submitted on: Dec 28, 2012
Accepted on: Feb 26, 2013
Published on: Jul 25, 2013
Published by: Columbia University Libraries/Information Services
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2013 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, published by Columbia University Libraries/Information Services
This work is licensed under the Creative Commons License.