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Q37615597-5CC41FA5-1747-4E59-AC93-C2D90238B944
Q37615597-5CC41FA5-1747-4E59-AC93-C2D90238B944
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Statement
http://www.wikidata.org/entity/statement/Q37615597-5CC41FA5-1747-4E59-AC93-C2D90238B944
Compound Heterozygote Mutation of C12orf65 Causes Distal Motor Neuropathy and Optic Atrophy
P2860
Q37615597-5CC41FA5-1747-4E59-AC93-C2D90238B944
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37615597-5CC41FA5-1747-4E59-AC93-C2D90238B944
rank
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Statement
wasDerivedFrom
9352afe3064aaf720b2464c686213c3ca34f1504
P2860
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).