Cargando…
Identification of a Rare Novel KMT2C Mutation That Presents with Schizophrenia in a Multiplex Family
Schizophrenia is a complex genetic disorder involving many common variants with modest effects and rare mutations with high penetrance. Rare mutations associated with schizophrenia are highly heterogeneous and private for affected individuals and families. Identifying such mutations can help establi...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707139/ https://www.ncbi.nlm.nih.gov/pubmed/34945726 http://dx.doi.org/10.3390/jpm11121254 |