Laminopathies.
作者信息
Lattanzi Giovanna, Maggi Lorenzo, Araujo-Vilar David
机构信息
a CNR Institute of Molecular Genetics , Unit of Bologna , Bologna , Italy.
b Rizzoli Orthopedic Institute , Bologna , Italy.
出版信息
Nucleus. 2018;9(1):543-544. doi: 10.1080/19491034.2018.1515606.
Abstract
摘要
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本文引用的文献
1
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.编码核纤层蛋白A/C的基因突变会导致常染色体显性遗传的埃默里-德赖富斯肌营养不良症。
Nat Genet. 1999 Mar;21(3):285-8. doi: 10.1038/6799.
2
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy.鉴定一个导致埃默里-德赖富斯肌营养不良症的新的X连锁基因。
Nat Genet. 1994 Dec;8(4):323-7. doi: 10.1038/ng1294-323.
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