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A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures

At least 5% of children present unexpected difficulties in expressing and understanding spoken language. This condition is highly heritable and often co-occurs with other neurodevelopmental disorders such as dyslexia and ADHD. Through an exome sequencing analysis, we identified a rare missense varia...

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Detalles Bibliográficos
Autores principales:	Martinelli, Angela, Rice, Mabel L, Talcott, Joel B, Diaz, Rebeca, Smith, Shelley, Raza, Muhammad Hashim, Snowling, Margaret J, Hulme, Charles, Stein, John, Hayiou-Thomas, Marianna E, Hawi, Ziarih, Kent, Lindsey, Pitt, Samantha J, Newbury, Dianne F, Paracchini, Silvia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	General Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188402/ https://www.ncbi.nlm.nih.gov/pubmed/33864365 http://dx.doi.org/10.1093/hmg/ddab111

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