Autism

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.

3 Sep , 2015 News from the world

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.

J Neurodev Disord. 2015 Aug 6 Authors Hu J, Liao J, Sathanoori M, Kochmar S, Sebastian J, Yatsenko SA, Surti U. Abstract Neurodevelopmental disorders are impairments of brain function that affect emotion, learning, and memory. Copy number variations of contactin genes (CNTNs), including CNTN3, CNTN4, CNTN5, and CNTN6, have been suggested to be associated with these disorders. However, phenotypes have been […]

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New publication on HMG!

31 Jan , 2014 News from Microgenomics

New publication on HMG!

Microgenomics Staff invites you to read an interesting paper, published on Human Molecular Genetics Journal, it is the result of a collaboration between several European centers. In this work A.C. Lionel and his colleagues have focused on the study of Copy Number Variation in 9q33.1 and rare map that involves the gene ASTN2. This gene […]

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