Genotype–Phenotype Relations for the Atypical Parkinsonism Genes:MDSGene Systematic Review

This Movement Disorder Society Genetic mutation database Systematic Review focuses on monogenic atypical parkinsonism with mutations in the ATP13A2, DCTN1, DNAJC6, FBXO7, SYNJ1, and VPS13C genes. We screened 673 citations and extracted genotypic and phenotypic data for 140 patients (73 families) fro...

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Detalles Bibliográficos
Autores principales: Wittke, Christina, Petkovic, Sonja, Dobricic, Valerija, Schaake, Susen, Respondek, Gesine, Weissbach, Anne, Madoev, Harutyun, Trinh, Joanne, Vollstedt, Eva-Juliane, Kuhnke, Neele, Lohmann, Katja, Dulovic Mahlow, Marija, Marras, Connie, König, Inke R., Stamelou, Maria, Bonifati, Vincenzo, Lill, Christina M., Kasten, Meike, Huppertz, Hans-Jürgen, Höglinger, Günter, Klein, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070562/
https://www.ncbi.nlm.nih.gov/pubmed/34396589
http://dx.doi.org/10.1002/mds.28517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070562/
https://www.ncbi.nlm.nih.gov/pubmed/34396589
http://dx.doi.org/10.1002/mds.28517

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