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Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability
Intellectual disability (ID) affects up to 2% of the population world-wide and often coincides with other neurological conditions such as autism spectrum disorders. Mutations in KDM5C cause Mental Retardation, X-linked, Syndromic, Claes-Jensen type (MRXSCJ, OMIM #300534) and are one of the most comm...
Autores principales: | Vallianatos, Christina N., Farrehi, Clara, Friez, Michael J., Burmeister, Margit, Keegan, Catherine E., Iwase, Shigeki |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893713/ https://www.ncbi.nlm.nih.gov/pubmed/29670509 http://dx.doi.org/10.3389/fnmol.2018.00104 |
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