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A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion
Deletions in the 2p16.3 region that includes the neurexin (NRXN1) gene are associated with intellectual disability and various psychiatric disorders, in particular, autism and schizophrenia. We present three unrelated patients, two adults and one child, in whom we identified an intragenic 2p16.3 del...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BlackWell Publishing Ltd
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4303221/ https://ncbi.nlm.nih.gov/pubmed/25614873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.105 |
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