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J Appl Phys 113

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

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Biochem J 2002

There are also similar studies focusing on the nature of binding of neurexins and LRRTMs, the results of which support the existence of a Ca 2+ dependence of binding [61], similar to K + , may be involved in the regulation of variable splicing of neurexins, affecting the LNS6 structural domain of neurexins and thus influencing binding to the postsynaptic adhesion molecule neuroligins [83]