GRN mutation in a patient with a behavioral variant of frontotemporal lobar degeneration (bvFTD)

The clinical spectrum of frontotemporal lobar degeneration (FTLD) is characterized by personality changes, language impairment, and executive function deficits. About 40% of FTLD cases have a family history of the disease, and the GRN gene is currently the most frequent genetic determinant. In cases...

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Hlavní autoři:	Sylwia Walczysková, Pavel Ressner, Šárka Hilscherová, Jaroslav Kotlas, Jiří Konrád, Věnceslava Svobodová
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Termedia Publishing House 2017-03-01
Edice:	Folia Neuropathologica
Témata:	<i>caudate nucleus atrophy frontotemporal dementia GRN gene splicing mutation</i>
On-line přístup:	https://www.termedia.pl/GRN-mutation-in-a-patient-with-a-behavioral-variant-of-frontotemporal-lobar-degeneration-bvFTD-,20,29689,1,1.html
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