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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Chia-Hsiang, Huang, Ailing, Huang, Yu-Shu, Fang, Ting-Hsuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707139/
https://www.ncbi.nlm.nih.gov/pubmed/34945726
http://dx.doi.org/10.3390/jpm11121254

Ejemplares similares