المؤلفون: Weissbach, A, Pauly, MG, Herzog, R, Hahn, L, Halmans, S, Hamami, F, Bolte, C, Camargos, S, Jeon, B, Kurian, MA, Opladen, T, Brueggemann, N, Huppertz, H-J, Koenig, IR, Klein, C, Lohmann, K

المصدر: Movement Disorders (2021)

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, dopa-responsive dystonia, genetics, GCH1, TH, SPR, PTS, QDPR, MDSGene, automated classification, MUTATIONS, DEFICIENCY

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10141742/1/Kurian_Relationship%20of%20Genotype,%20Phenotype,%20and%20Treatment%20in%20Dopa-Responsive%20Dystonia_AOP.pdf; https://discovery.ucl.ac.uk/id/eprint/10141742/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10141742/1/Kurian_Relationship%20of%20Genotype,%20Phenotype,%20and%20Treatment%20in%20Dopa-Responsive%20Dystonia_AOP.pdf
https://discovery.ucl.ac.uk/id/eprint/10141742/