Isolated mitochondrial respiratory chain complex I deficiency (Q102302): Difference between revisions
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Trata-se da transferência de elétrons acoplada isolada entre um doador de elétrons (como NADH) e um aceptor de elétrons (como O2) com a transferência de íons H + (prótons) através de uma membrana. Este diagnóstico é com deficiência no Complexo I quando dois elétrons são removidos do NADH e transferidos para um carreador lipossolúvel, a ubiquinona (Q). | |||
| description / en | description / en | ||
This refers to isolated coupled electron transfer between an electron donor (such as NADH) and an electron acceptor (such as O2) with the transfer of H+ ions (protons) across a membrane. This diagnosis is with deficiency in Complex I when two electrons are removed from NADH and transferred to a lipid-soluble carrier, ubiquinone (Q). | |||
Revision as of 19:14, 16 August 2026
This refers to isolated coupled electron transfer between an electron donor (such as NADH) and an electron acceptor (such as O2) with the transfer of H+ ions (protons) across a membrane. This diagnosis is with deficiency in Complex I when two electrons are removed from NADH and transferred to a lipid-soluble carrier, ubiquinone (Q).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_67580224 |
||
| English | Isolated mitochondrial respiratory chain complex I deficiency |
This refers to isolated coupled electron transfer between an electron donor (such as NADH) and an electron acceptor (such as O2) with the transfer of H+ ions (protons) across a membrane. This diagnosis is with deficiency in Complex I when two electrons are removed from NADH and transferred to a lipid-soluble carrier, ubiquinone (Q). |
