Ontology highlight
ABSTRACT:
SUBMITTER: Gillentine MA
PROVIDER: S-EPMC5443344 | biostudies-literature | 2017 Mar
REPOSITORIES: biostudies-literature
Gillentine M A MA Berry L N LN Goin-Kochel R P RP Ali M A MA Ge J J Guffey D D Rosenfeld J A JA Hannig V V Bader P P Proud M M Shinawi M M Graham B H BH Lin A A Lalani S R SR Reynolds J J Chen M M Grebe T T Minard C G CG Stankiewicz P P Beaudet A L AL Schaaf C P CP
Journal of autism and developmental disorders 20170301 3
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 pathogenicity of duplications of CHRNA7 is unclear, as they are found in affected probands as well as in reportedly healthy parents and unaffected control individuals. We evaluated 18 children with mic ...[more]