The cognitive and behavioral phenotypes of individuals with CHRNA7 duplications

Chromosome 15q11q13 is among the least stable regions in the genome due to its highly complex genomic architecture. Low copy repeat elements at 15q13.3 facilitate recurrent copy number variants (CNVs), with deletions established as pathogenic and CHRNA7 implicated as a candidate gene. However, the p...

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Bibliografiset tiedot
Julkaisussa:J Autism Dev Disord
Päätekijät: Gillentine, MA, Berry, LN, Goin-Kochel, RP, Ali, MA, Ge, J, Guffey, D, Rosenfeld, JA, Hannig, V, Bader, P, Proud, M, Shinawi, M, Graham, BH, Lin, A, Lalani, SR, Reynolds, J, Chen, M, Grebe, T, Minard, CG, Stankiewicz, P, Beaudet, AL, Schaaf, CP
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5443344/
https://ncbi.nlm.nih.gov/pubmed/27853923
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10803-016-2961-8
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