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MT-ND1 gene mutation
Clinical significance:
- defects in MT-ND1 are a cause of
a) Leber hereditary optic neuropathy
b) MELAS syndrome
c) mitochondrial susceptibility to Alzheimer disease
d) non-insulin-dependent diabetes mellitus (NIDDM)
Related
NADH dehydrogenase subunit-1 (NADH ubiquinone oxidoreductase chain-1, MT-ND1, MTND1, NADH1, ND1)
General
gene mutation testing; gene mutation analysis
References
Loinc