mjd的近义词

Spinocerebellar ataxia type 3/ Machado-Joseph disease ( SCA3/ MJD) is a kind of autosomal dominant disease, which is characterized by degeneration of neurons and accumulation of aberrant protein aggregates in affected neurons.

脊髓小脑型共济失调Ⅲ型/马查多-约瑟夫病（SCA3/MJD），是一种以神经细胞变性、细胞核内蛋白聚集体形成为病理特征的常染色体显性遗传病。

Methods Family visiting, physical examination and the blood samples were analysed on molecular biology in 44 members of a family with MJD. The cases of inpatients were examined on cerebrospinal fluid and neuro electrophysiology.

方法对一MJD家系44名成员家访、体检、采静脉血作分子生物学分析，住院病例进行脑脊液及神经电生理检查。

The shortest repeats of ( CAG) 8 in alleles of SCA3/ MJD genes may be special genotype in northeastern of china.

我们首次发现大量的8个CAG三核昔酸重复拷贝，是目前所发现的在scA3/MJD基因中最短的重复拷贝数，它很可能是我国东北地区特有的等位基因型。