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Q39364834-1761A3B1-61E8-4CAD-B503-27C5DBB7894B
Q39364834-1761A3B1-61E8-4CAD-B503-27C5DBB7894B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-1761A3B1-61E8-4CAD-B503-27C5DBB7894B
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation.
P31
Q39364834-1761A3B1-61E8-4CAD-B503-27C5DBB7894B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-1761A3B1-61E8-4CAD-B503-27C5DBB7894B
rank
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type
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Statement
wasDerivedFrom
b65afc210436386f8df5d9b62b014247ffc34a5a
P31
scholarly article