A ubiquitin-like domain is required for stabilizing the N-terminal ATPase module of human SMCHD1

Variants in the gene SMCHD1, which encodes an epigenetic repressor, have been linked to both congenital arhinia and a late-onset form of muscular dystrophy called facioscapulohumeral muscular dystrophy type 2 (FSHD2). This suggests that SMCHD1 has a diversity of functions in both developmental time...

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Detalles Bibliográficos
Autores principales: Pedersen, Lars C., Inoue, Kaoru, Kim, Susan, Perera, Lalith, Shaw, Natalie D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620310/
https://www.ncbi.nlm.nih.gov/pubmed/31312724
http://dx.doi.org/10.1038/s42003-019-0499-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620310/
https://www.ncbi.nlm.nih.gov/pubmed/31312724
http://dx.doi.org/10.1038/s42003-019-0499-y

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