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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2019
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| Materias: | |
| 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 |