The Whole Exome Sequencing Clarifies the Genotype- Phenotype Correlations in Patients with Early-Onset Dementia

Our study aimed to identify the underlying causes in patients with early onset dementia by clinical and genetic exploration. We recruited a group of 38 patients with early-onset dementia. Firstly, hexanucleotide repeat expansions in C9ORF72 gene were screened in all subjects to exclude the possibili...

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Detalhes bibliográficos
Publicado no:Aging Dis
Main Authors: Xu, Yangqi, Liu, Xiaoli, Shen, Junyi, Tian, Wotu, Fang, Rong, Li, Binyin, Ma, Jianfang, Cao, Li, Chen, Shengdi, Li, Guanjun, Tang, Huidong
Formato: Artigo
Idioma:Inglês
Publicado em: JKL International LLC 2018
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Orginal Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6065298/
https://ncbi.nlm.nih.gov/pubmed/30090657
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14336/AD.2018.0208
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