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Q33649447-B9A10359-6DE5-49E6-9C23-CE1F4654CEA3
Q33649447-B9A10359-6DE5-49E6-9C23-CE1F4654CEA3
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http://www.wikidata.org/entity/statement/Q33649447-B9A10359-6DE5-49E6-9C23-CE1F4654CEA3
Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression.
P2860
Q33649447-B9A10359-6DE5-49E6-9C23-CE1F4654CEA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33649447-B9A10359-6DE5-49E6-9C23-CE1F4654CEA3
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wasDerivedFrom
a6d637cf95dac67451fba2f5045fb892288344ce
P2860
Loss of Mfn2 results in progressive, retrograde degeneration of dopaminergic neurons in the nigrostriatal circuit.