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Trapping MBD5 to understand 2q23.1 microdeletion syndrome
Despite genetic evidence implicating MBD5 as the only overlapping gene between various 2q23.1 microdeletions, the function of MBD5 and its causality to 2q23.1 microdeletion syndrome, a disorder characterized by developmental delay and autistic features, has yet to be determined. In this issue of EMB...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BlackWell Publishing Ltd
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4154127/ https://ncbi.nlm.nih.gov/pubmed/25001217 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201404324 |
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