Reply: Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease.

Gerards, Mike; de Coo, René; Smeets, Hubert

Gerards, Mike; de Coo, René; Smeets, Hubert.

Afiliación

Gerards M; 1 Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, Maastricht, The Netherlands2 School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands3 Biomeditech and Tampere University Hospital, University of Tampere, FI-33014, Finland Mike.Gerards@maastrichtuniversity.nl.
de Coo R; 4 Department of Neurology, Erasmus MC, Rotterdam, The Netherlands.
Smeets H; 1 Department of Clinical Genetics, Unit Clinical Genomics, Maastricht University Medical Centre, Maastricht, The Netherlands2 School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.

Brain ; 137(Pt 9): e296, 2014 Sep.

Article en En | MEDLINE | ID: mdl-24878501

Asunto(s)

Exoma/genética; Enfermedad de Leigh/genética; Proteínas de Transporte de Membrana/genética; Femenino; Humanos; Masculino

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Transporte de Membrana / Enfermedad de Leigh / Exoma Límite: Female / Humans / Male Idioma: En Revista: Brain Año: 2014 Tipo del documento: Article País de afiliación: Finlandia

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