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Q39364834-88F95F38-9868-44C6-B533-E9212BCB55E7
Q39364834-88F95F38-9868-44C6-B533-E9212BCB55E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-88F95F38-9868-44C6-B533-E9212BCB55E7
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation.
P1476
Q39364834-88F95F38-9868-44C6-B533-E9212BCB55E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-88F95F38-9868-44C6-B533-E9212BCB55E7
rank
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type
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wasDerivedFrom
b65afc210436386f8df5d9b62b014247ffc34a5a
P1476
Isolated late-onset cone-rod d
......
T8993G mitochondrial mutation
@en