ロード中...
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...
保存先:
出版年: | Commun Biol |
---|---|
主要な著者: | , , , , |
フォーマット: | Artigo |
言語: | Inglês |
出版事項: |
Nature Publishing Group UK
2019
|
主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6620310/ https://ncbi.nlm.nih.gov/pubmed/31312724 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s42003-019-0499-y |
タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|