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1
Q55383192-C5F4E372-9AEB-48B8-B87B-512427BB369B
Q55383192-C5F4E372-9AEB-48B8-B87B-512427BB369B
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Statement
http://www.wikidata.org/entity/statement/Q55383192-C5F4E372-9AEB-48B8-B87B-512427BB369B
ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.
P2860
Q55383192-C5F4E372-9AEB-48B8-B87B-512427BB369B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55383192-C5F4E372-9AEB-48B8-B87B-512427BB369B
rank
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Statement
wasDerivedFrom
8404f3e303aa3c6bccd37b98dd12394ad39ca147
P2860
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).