Properties of ATP6 mutant strains.
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资源简介：
The atp6-L183R mutation is homologous to human T8993G/L156R, the most frequent mutation associated to neurogenic ataxia retinitis pigmentosa (NARP). The atp6-L247R mutation is homologous to human T9176G/L217R, which is associated to maternally-inherited Leigh syndrome (MILS), the most severe form of NARP. *COX activity was extimated by measuring oxygen consumption with ascorbate/TMPD (N,N,N’,N’-tetramethyl-p-phenylenediamine), that directly reduce cytochrome c.
创建时间：
2015-12-02
