Mutation analysis of patients with Neurodegenerative disorders using NeuroX array

Genetic analyses of patients with neurodegenerative disorders have identified multiple genes that need to be investigated for the presence of damaging variants. However, mutation analysis by Sanger sequencing is costly and time consuming. We tested the utility of a recently designed semi-custom geno...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Neurobiol Aging
Päätekijät: Ghani, Mahdi, Lang, Anthony E, Zinman, Lorne, Nacmias, Benedetta, Sorbi, Sandro, Tartaglia, Maria Carmela, Surace, Ezequiel I, Sato, Christine, Moreno, Danielle, Xi, Zhengrui, Hung, Rachel, Nalls, Mike A, Singleton, Andrew, George-Hyslop, Peter St, Rogaeva, Ekaterina
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2014
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4268030/
https://ncbi.nlm.nih.gov/pubmed/25174650
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2014.07.038
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