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Mutación de novo en DYNC1H1, atrofia muscular espinal y problemas atencionales / DYNC1H1 de novo mutation, spinal muscular atrophy and attention problems
Fernández Perrone, A. L; Moreno Fernández, P; Álvarez, S; Fernández-Jaén, A.
Affiliation
  • Fernández Perrone, A. L; Hospital Universitario Quirónsalud. Departamento de Neuropediatría. Madrid. España
  • Moreno Fernández, P; Hospital Universitario Quirónsalud. Laboratorio de Electromiografía. Madrid. España
  • Álvarez, S; NIMGenetics. Genómica y Medicina. Madrid. España
  • Fernández-Jaén, A; Hospital Universitario Quirónsalud. Universidad Europea de Madrid. Madrid. España
Neurología (Barc., Ed. impr.) ; 37(5): 406-409, Jun. 2022. ilus
Article in English, Spanish | IBECS | ID: ibc-205991
Responsible library: ES1.1
Localization: ES15.1 - BNCS
Fulltext

Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Muscular Atrophy, Spinal / Charcot-Marie-Tooth Disease Limits: Humans Language: English / Spanish Journal: Neurología (Barc., Ed. impr.) Year: 2022 Document type: Article Institution/Affiliation country: Hospital Universitario Quirónsalud/España / NIMGenetics/España
Fulltext

Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Muscular Atrophy, Spinal / Charcot-Marie-Tooth Disease Limits: Humans Language: English / Spanish Journal: Neurología (Barc., Ed. impr.) Year: 2022 Document type: Article Institution/Affiliation country: Hospital Universitario Quirónsalud/España / NIMGenetics/España
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