Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population

The Forkhead box P2 (FOXP2) is an evolutionary conserved transcription factor involved in the maintenance of neuronal networks, implicated in language disorders. Some evidence suggests a possible link between FOXP2 genetic variability and frontotemporal dementia (FTD) pathology and related endopheno...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Paolina Crocco, Francesco De Rango, Francesco Bruno, Antonio Malvaso, Raffaele Maletta, Amalia C. Bruni, Giuseppe Passarino, Giuseppina Rose, Serena Dato
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Elsevier 2024-06-01
Sarja:	Heliyon
Aiheet:	Frontotemporal dementia FTD FOXP2 PRNP CNTNAP2 SNPs
Linkit:	http://www.sciencedirect.com/science/article/pii/S2405844024076552
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