SDHA gene mutation
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Contents
1
Clinical significance
2
More general terms
3
Additional terms
4
References
Clinical significance
SDHA
mutations
are a cause of
succinate CoQ reductase deficiency
Leigh syndrome
More general terms
gene mutation testing; gene mutation analysis
Additional terms
succinate dehydrogenase flavoprotein subunit (SDHA, SDH2, SDHF)
References
↑
Loinc
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