Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency. Dominguez-Gonzalez C, et al. #EHUpaper in Orphanet Journal of Rare Diseases https://t.co/kcdgHdrklp https://t.co/KKLnU9lDYc
1,373 followers
2,163 followers
Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency https://t.co/6hEHygagCQ
2,357 followers
Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 … https://t.co/eZX2hQtBcU #hvhebron #ped [Text complet] @ojrarediseases
1,959 followers
Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 … https://t.co/wRYrk8wzg1 . Hospital Materno Infantil de Badajoz (Neurología)