NRXN1 Deletion in Two Twins’ Genotype and Phenotype: A Clinical Case and Literature Review
In the literature, deletions in the 2p16.3 region of the neurexin gene (NRXN1) are associated with cognitive impairment, and other neuropsychiatric disorders, such as schizophrenia, autism, and Pitt–Hopkins-like syndrome 2. In this paper, we present twins with deletion 2p16.3 of the NRXN1 gene using...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI AG
2022-05-01
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| coleção: | Children |
| Assuntos: | |
| Acesso em linha: | https://www.mdpi.com/2227-9067/9/5/698 |
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