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- W2083414819 abstract "The purpose of this review is to provide a comprehensive update on the genetic causes of frontotemporal lobar degeneration (FTLD). Approximately 40% to 50% of patients diagnosed with FTLD have a family history of a ‘‘related disorder,’’ whereas 10% to 40% have an autosomal dominant family history for the disease. At this time, mutations occurring in 2 independent genes located on the same chromosome (MAPT and GRN) have been shown to cause the majority of cases of autosomal dominant FTLD. Specific genetic, molecular, pathological, and phenotypic variations associated with each of these gene mutations are discussed, as well as markers that may help differentiate the 2. In addition, 3 relatively rare, additional genes known to cause familial FTLD are examined in brief. Lastly, genetic counseling issues which may be important to the community clinician are discussed." @default.
- W2083414819 created "2016-06-24" @default.
- W2083414819 creator A5046120768 @default.
- W2083414819 creator A5050149439 @default.
- W2083414819 creator A5060985442 @default.
- W2083414819 creator A5071338087 @default.
- W2083414819 date "2010-10-11" @default.
- W2083414819 modified "2023-09-27" @default.
- W2083414819 title "Genetic Causes of Frontotemporal Degeneration" @default.
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- W2083414819 doi "https://doi.org/10.1177/0891988710383574" @default.
- W2083414819 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20938042" @default.
- W2083414819 hasPublicationYear "2010" @default.
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