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Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

In order to assess the frequency of mutations in the known Alzheimer's disease causative genes in Turkish dementia patients we screened amyloid precursor protein (APP), PSEN1 and PSEN2 for mutations in a cohort of 98 Turkish dementia families. Six families were found to carry PSEN1 mutations (p...

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Dades bibliogràfiques
Publicat a:Neurobiol Aging
Autors principals: Lohmann, Ebba, Guerreiro, Rita J., Erginel-Unaltuna, Nihan, Gurunlian, Nicole, Bilgic, Basar, Gurvit, Hakan, Hanagasi, Hasmet A., Luu, Nga, Emre, Murat, Singleton, Andrew
Format: Artigo
Idioma:Inglês
Publicat: 2012
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4669567/
https://ncbi.nlm.nih.gov/pubmed/22503161
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2012.02.020
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