HOSPITAL UNIVERSITARIO INFANTA SOFÍA
Department
Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaPublications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Raras (2)
2017
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Genetic polymorphisms of SCN9A are associated with oxaliplatin-induced neuropathy
BMC Cancer, Vol. 17, Núm. 1
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Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes
PLoS ONE, Vol. 12, Núm. 11