Conclusion Abore point mutation is an inherited gene mutation.

结论表明该突变为一遗传性突变.

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Result: We had not point mutation in all subjects.

结果: 所有对象均未检测到点突变.

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Conclusion: The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia.

结论: 遗传性共济失调的发生、发展可能与该区域点突变无关.

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A point mutation is foundin two patients at nucleotide 31119 , resulting in G ( CGA ) to A ( CAA ).

发现这两例都发生在31119位的碱基替换, G ( CGA ) →A ( CAA ).

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