Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population-Reference-Cited by-同舟云学术

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

Published:2024-06 Issue:11 Volume:10 Page:e31624
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Crocco Paolina,De Rango Francesco,Bruno Francesco,Malvaso Antonio,Maletta Raffaele,Bruni Amalia C.,Passarino Giuseppe,Rose Giuseppina,Dato Serena^ORCID

Funder

MIUR

Publisher

Elsevier BV

Reference60 articles.

1. Human-specific transcriptional regulation of CNS development genes by FOXP2;Konopka;Nature,2009

2. Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain;Spiteri;Am. J. Hum. Genet.,2007

3. Localisation of a gene implicated in a severe speech and language disorder;Fisher;Nat. Genet.,1998

4. FOXP2-Related speech and language disorder;Morgan,2016

5. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum;Reuter;J. Med. Genet.,2017

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