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Functional genomics analysis of Phelan-McDermid syndrome 22q13 region during human neurodevelopment
Phelan-McDermid syndrome (PMS) is a neurodevelopmental disorder characterized by varying degrees of intellectual disability, severely delayed language development and specific facial features, and is caused by a deletion within chromosome 22q13.3. SHANK3, which is located at the terminal end of this...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420160/ https://www.ncbi.nlm.nih.gov/pubmed/30875393 http://dx.doi.org/10.1371/journal.pone.0213921 |