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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