Human Genome Epidemiology Literature Finder
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Query Trace: Language Disorders and CNTNAP2[original query] |
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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. Heliyon 2024 6 10 (11): e31624. Paolina Crocco, Francesco De Rango, Francesco Bruno, Antonio Malvaso, Raffaele Maletta, Amalia C Bruni, Giuseppe Passarino, Giuseppina Rose, Serena Da |
- Page last reviewed:Feb 1, 2024
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