Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| 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 |
| Investigating Sequence Variations in CNTNAP2 and SETBP1 Genes in Language Disorders. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2025 1 23 (1): 100-109. Betül Turan, Emine Gökta?, Necati Uzun, Ay?egül Tu?ba H?ra Selen, Ay?e Gül Zamani, Mahmut Selman Y?ld?r |
- Page last reviewed:Feb 1, 2024
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