首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene.
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A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene.

机译:一个新的突变,代表芳基硫酸酯酶A基因的编码序列中的第五个非致病性多态性。

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摘要

A novel mutation, a C-->T transition at nucleotide 455 of the coding sequence of the ARSA gene, was found in a control individual during the search for metachromatic leukodystrophy mutations. Its distribution in three different populations was examined. The frequency of the T allele was 0.058, 0.025 and 0.033, in Italian, German and Greek populations, respectively. The mutation results in no amino acid substitution and can be identified as it creates a a polymorphic site for the restriction endonuclease N/aIII.
机译:在寻找亚型的白细胞营养不良突变的对照个体中,发现了一个新的突变,即ARSA基因编码序列的核苷酸455处的C→T过渡。检查了它在三个不同人群中的分布。在意大利,德国和希腊人群中,T等位基因的频率分别为0.058、0.025和0.033。该突变不会导致氨基酸取代,并且可以被识别,因为它为限制性核酸内切酶N / aIII创建了一个多态位点。

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