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A Clinical, Molecular Genetics and Pathological Study of a FTDP-17 Family with a Heterozygous Splicing Variant C.823-10G>t at the Intron 9/exon 10 of the MAPT Gene.

Diana A. Olszewska,Conor Fearon,Christopher McGuigan,Terri P. McVeigh,Henry Houlden,James M. Polke,Brian Lawlor,Robert Coen,Michael Hutchinson,Michael Hutton,Alan Beausang,Isabelle Delon,Francesca Brett,Ioanna Sevastou,Nuria Seto-Salvia,Rohan de Silva,Tim Lynch

Neurobiology of aging（2024）

引用 4|浏览30
关键词
c.823-10G>T,Intron 9/exon 10 mutation,Frontotemporal dementia,Genetics,Neuropathology
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