Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency

  1. Domínguez-González, C.
  2. Madruga-Garrido, M.
  3. Hirano, M.
  4. Martí, I.
  5. Martín, M.A.
  6. Munell, F.
  7. Nascimento, A.
  8. Olivé, M.
  9. Quan, J.
  10. Sardina, M.D.
  11. Martí, R.
  12. Paradas, C.
Revue:
Orphanet Journal of Rare Diseases

ISSN: 1750-1172

Année de publication: 2021

Volumen: 16

Número: 1

Type: Révision

DOI: 10.1186/S13023-021-02030-W GOOGLE SCHOLAR lock_openAccès ouvert editor

Objectifs de Développement Durable

La source de données: Scopus