De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability

De novo mutations (DNM) in SYNGAP1, encoding Ras/Rap GTPase‐activating protein SynGAP, have been reported in individuals with nonsyndromic intellectual disability (ID). We identified 10 previously unreported individuals with SYNGAP1 DNM; seven via the Deciphering Developmental Disorders (DDD) Study,...

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Detalles Bibliográficos
Autores principales: Parker, Michael J., Fryer, Alan E., Shears, Deborah J., Lachlan, Katherine L., McKee, Shane A., Magee, Alex C., Mohammed, Shehla, Vasudevan, Pradeep C., Park, Soo‐Mi, Benoit, Valérie, Lederer, Damien, Maystadt, Isabelle, study, DDD, FitzPatrick, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
New Syndrome
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744742/
https://www.ncbi.nlm.nih.gov/pubmed/26079862
http://dx.doi.org/10.1002/ajmg.a.37189

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744742/
https://www.ncbi.nlm.nih.gov/pubmed/26079862
http://dx.doi.org/10.1002/ajmg.a.37189

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