Publications in collaboration with researchers from Complejo Hospitalario Universitario de Albacete (3)

2020

  1. Paucisymptomatic hyperCKemia due to a mutation in the ANO5 gene

    Neurologia

2015

  1. Corrigendum to "Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening" [Mol. Genet. Metab. 110 (2013) 218-221]

    Molecular Genetics and Metabolism

2013

  1. Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening

    Molecular Genetics and Metabolism, Vol. 110, Núm. 3, pp. 218-221