Literature DB >> 27215640

Duplication of FOXP2 binding sites within CNTNAP2 gene in a girl with neurodevelopmental delay.

Renato Polimanti1, Rosanna Squitti2,3, Marilena Pantaleo4, Sabrina Giglio4, Giancarlo Zito5,6.   

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Year:  2016        PMID： 27215640     DOI： 10.23736/S0026-4946.16.04326-7

Source DB:  PubMed          Journal:  Minerva Pediatr        ISSN： 0026-4946            Impact factor:   1.312


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  3 in total

Review 1.  Intragenic CNTNAP2 Deletions: A Bridge Too Far?

Authors:  Martin Poot
Journal:  Mol Syndromol       Date:  2017-02-10

2.  19q12q13.2 duplication syndrome: neuropsychiatric long-term follow-up of a new case and literature update.

Authors:  Renata Nacinovich; Nicoletta Villa; Fiorenza Broggi; Cristina Tavaniello; Monica Bomba; Donatella Conconi; Serena Redaelli; Elena Sala; Marialuisa Lavitrano; Francesca Neri
Journal:  Neuropsychiatr Dis Treat       Date:  2017-10-04       Impact factor: 2.570

3.  Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.

Authors:  Claudio Toma; Kerrie D Pierce; Alex D Shaw; Anna Heath; Philip B Mitchell; Peter R Schofield; Janice M Fullerton
Journal:  PLoS Genet       Date:  2018-12-26       Impact factor: 5.917
  3 in total

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