mjd的音标

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。

Results The gene mutations of 9 SCA families were MJD among which 6 asymptomatic MJD had been detected in 2 SCA families.

结果检出9个家系为MJD，其中2个MJD家系检测到6例症状前MJD。