Three brothers with a nonsense mutation in KAT6A caused by parental germline mosaicism

Mutations in KAT6A, encoding a member of the MYST family of histone acetyl-transferases, were recently reported in patients with a neurodevelopmental disorder (OMIM: #616268, autosomal dominant mental retardation-32). In this report, we describe three siblings with intellectual disability (ID) or gl...

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Detalles Bibliográficos
Autores principales: Satoh, Chisei, Maekawa, Ryuta, Kinoshita, Akira, Mishima, Hiroyuki, Doi, Michiko, Miyazaki, Mutsuko, Fukuda, Masafumi, Takahashi, Haruo, Kondoh, Tatsuro, Yoshiura, Koh-ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863403/
https://www.ncbi.nlm.nih.gov/pubmed/31754438
http://dx.doi.org/10.1038/hgv.2017.45

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