Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

Copy number variants (CNVs) at chromosome 16p13.11 have been associated with a range of neurodevelopmental disorders including autism, ADHD, intellectual disability and schizophrenia. Significant sex differences in prevalence, course and severity have been described for a number of these conditions...

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Autores principales:	Maria Tropeano, Joo Wook Ahn, Richard J B Dobson, Gerome Breen, James Rucker, Abhishek Dixit, Deb K Pal, Peter McGuffin, Anne Farmer, Peter S White, Joris Andrieux, Evangelos Vassos, Caroline Mackie Ogilvie, Sarah Curran, David A Collier
Formato:	article
Lenguaje:	EN
Publicado:	Public Library of Science (PLoS) 2013
Materias:	Medicine R Science Q
Acceso en línea:	https://doaj.org/article/49c7f56bc6bd4332b987a49bb5d588de
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Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

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