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Detection of Rare Methyl-CpG Binding Protein 2 Gene Missense Mutations in Patients With Schizophrenia

Deleterious mutations of MECP2 are responsible for Rett syndrome, a severe X-linked childhood neurodevelopmental disorder predominates in females, male patients are considered fatal. However, increasing reports indicate that some MECP2 mutations may also present various neuropsychiatric phenotypes,...

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Dades bibliogràfiques
Publicat a:Front Genet
Autors principals: Chen, Chia-Hsiang, Cheng, Min-Chih, Huang, Ailing, Hu, Tsung-Ming, Ping, Lieh-Yung, Chang, Yu-Syuan
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7227600/
https://ncbi.nlm.nih.gov/pubmed/32457807
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00476
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