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MT-ND6 gene mutation
Clinical significance:
- defects in MT-ND6 are a cause of
a) Leber hereditary optic neuropathy
b) Leber optic atrophy & dystonia
c) MELAS syndrome
Related
NADH dehydrogenase subunit-6 (MT-ND6)
General
gene mutation testing; gene mutation analysis
References
Loinc