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Comment
. 2015 Sep;23(9):1113.
doi: 10.1038/ejhg.2014.262. Epub 2014 Dec 24.

ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis

Marcus Pembrey  1 , Jean Golding  2 , Jessica Connelly  3
Affiliations
Comment

ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis

Marcus Pembrey et al. Eur J Hum Genet. 2015 Sep.
No abstract available

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Comment in

Comment on

  • Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
    Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H; IMGSAC; SLI Consortium; WGS500 Consortium; Parr J, Pagnamenta AT, Maestrini E, Bacchelli E, Fisher SE, Newbury DF. Ceroni F, et al. Eur J Hum Genet. 2014 Oct;22(10):1165-71. doi: 10.1038/ejhg.2014.4. Epub 2014 Feb 12. Eur J Hum Genet. 2014. PMID: 24518835 Free PMC article.

References

    1. Ceroni F, Simpson NH, Francks C et al: Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. Eur J Hum Genet 2014; 22: 1165–1171. - PMC - PubMed
    1. Bucan M, Abrahams BS, Wang K et al: Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet 2009; 5: e1000536. - PMC - PubMed
    1. Golding J, Steer C, Pembrey M: Parental and Grandparental Ages in the Autistic Spectrum Disorders: A Birth Cohort Study. PLoS One 2010; 5: e9939. - PMC - PubMed
    1. Walsh CP, Chaillet JR, Bestor TH: Transcription of IAP endogenous retroviruses is constrained by cytosine methylation. Nat Genet 1998; 20: 116–117. - PubMed
    1. Gregory SG, Connelly JJ, Towers AJ et al: Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Med 2009; 7: 62. - PMC - PubMed

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