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

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2020-10-01

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Paradas, C.
Dominguez-Gonzalez, C.
Madruga-Garrido, M.
Hirano, M.
Marti, I.
Munell, F.
Nascimento, A.
Olive, M.
Quan, J.
Sardina, D.

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Pergamon-elsevier science ltd
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