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Exploring the behavioral and cognitive phenotype of KBG syndrome
KBG syndrome is a neurodevelopmental disorder, caused by dominant mutations in ANKRD11, that is characterized by developmental delay/intellectual disability, mild craniofacial dysmorphisms, and short stature. Behavior and cognition have hardly been studied, but anecdotal evidence suggests higher fre...
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| Publicado no: | Genes Brain Behav |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6850621/ https://ncbi.nlm.nih.gov/pubmed/30786142 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/gbb.12553 |
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