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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Detalles Bibliográficos
Autores principales: Sciacca, Monica, Marino, Lidia, Vitaliti, Giovanna, Falsaperla, Raffaele, Marino, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139251/
https://www.ncbi.nlm.nih.gov/pubmed/35626875
http://dx.doi.org/10.3390/children9050698

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139251/
https://www.ncbi.nlm.nih.gov/pubmed/35626875
http://dx.doi.org/10.3390/children9050698

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