Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability

Intellectual Disability (ID) is a clinically heterogeneous condition that affects 2–3% of population worldwide. In recent years, exome sequencing has been a successful strategy for studies of genetic causes of ID, providing a growing list of both candidate and validated ID genes. In this study, exom...

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Detalles Bibliográficos
Autores principales: Zhao, Jin J., Halvardson, Jonatan, Zander, Cecilia S., Zaghlool, Ammar, Georgii‐Hemming, Patrik, Månsson, Else, Brandberg, Göran, Sävmarker, Helena E., Frykholm, Carina, Kuchinskaya, Ekaterina, Thuresson, Ann‐Charlotte, Feuk, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765476/
https://www.ncbi.nlm.nih.gov/pubmed/28990276
http://dx.doi.org/10.1002/ajmg.b.32574

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765476/
https://www.ncbi.nlm.nih.gov/pubmed/28990276
http://dx.doi.org/10.1002/ajmg.b.32574

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