目的研究线粒体dna点突变与遗传性共济失调(HA)的关系。
Objective to study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia (HA).
并对4个突变点的成因进行了解释。
An explanation has been given to the formative cause of the 4 breaks.
其中16个突变位点未见过报道。
The mutations at 16 positions were found for the first time.
本研究从HBV基因突变入手，进一步探讨可能与宫内感染发生有关的突变位点。
Some gene position's mutation might have association with the HBV intrauterine infection.
本研究从HBV基因突变入手，进一步探讨可能与宫内感染发生有关的突变位点。
Some gene position's mutation might have association with the HBV intrauterine infection.
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