Tatton-Brown-Rahman syndrome with a novel DNMT3A mutation presented severe intellectual disability and autism spectrum disorder

Tatton-Brown-Rahman syndrome is a congenital anomaly syndrome that manifests with overgrowth, macrocephaly, and characteristic facial features. This autosomal dominant disease is caused by a germline mutation in DNMT3A. Some patients with this syndrome develop mild to severe intellectual disability,...

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Detalles Bibliográficos
Autores principales: Yokoi, Takayuki, Enomoto, Yumi, Naruto, Takuya, Kurosawa, Kenji, Higurashi, Norimichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235239/
https://www.ncbi.nlm.nih.gov/pubmed/32435502
http://dx.doi.org/10.1038/s41439-020-0102-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235239/
https://www.ncbi.nlm.nih.gov/pubmed/32435502
http://dx.doi.org/10.1038/s41439-020-0102-6

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