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

Paradas, C.Dominguez-Gonzalez, C.Madruga-Garrido, M.Hirano, M.Marti, I.Munell, F.Nascimento, A.Olive, M.Quan, J.Sardina, D.Marti, R.2025-01-072025-01-072020-10-010960-8966https://hdl.handle.net/10668/27255enCollaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiencyconference output10.1016/j.nmd.2020.08.3121873-2364579727800305