Mimault C, Cailloux F, Giraud G, Dastugue B, Boespflug-Tanguy O
INSERM U384, Faculté de Médecine, Clermont-Ferrand, France.
Hum Genet. 1995 Aug;96(2):236. doi: 10.1007/BF00207388.
We report a dinucleotide polymorphism in the first intron of the proteolipid protein (PLP) gene with a heterozygosity frequency of 0.69 useful for molecular analysis of families with X-linked neurologic disorders characterized by dysmyelination of the central nervous system, Pelizaeus-Merzbacher Disease (PMD) and X-linked Spastic Paraplegia (SPG2).
我们报道了蛋白脂质蛋白(PLP)基因第一个内含子中的一个二核苷酸多态性,其杂合频率为0.69,这对于以中枢神经系统髓鞘形成异常为特征的X连锁神经系统疾病、佩利措伊斯-梅茨巴赫病(PMD)和X连锁痉挛性截瘫(SPG2)家系的分子分析很有用。