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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

A. Macaya

Grup de Recerca en Malalties Neurometabòliques

Hospital Universitari Vall d'Hebron




Name/email consistency: high



  • Grup de Recerca en Malalties Neurometabòliques, Hospital Universitari Vall d'Hebron, Barcelona, Spain. 2005


  1. Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study. Macaya, A., Brunso, L., Fernández-Castillo, N., Arranz, J.A., Ginjaar, H.B., Cuenca-León, E., Corominas, R., Roig, M., Cormand, B. Neuropediatrics (2005) [Pubmed]
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