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Q24633194-2AD0BDDD-2517-4305-AB24-224C54F908E5
Q24633194-2AD0BDDD-2517-4305-AB24-224C54F908E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24633194-2AD0BDDD-2517-4305-AB24-224C54F908E5
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively
P2860
Q24633194-2AD0BDDD-2517-4305-AB24-224C54F908E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24633194-2AD0BDDD-2517-4305-AB24-224C54F908E5
rank
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type
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Statement
wasDerivedFrom
1b39253345bebd50c399ee7cecfb36dd6582319e
P2860
Molecular characterization of the human gene encoding an abundant 61 kDa protein specific to the retinal pigment epithelium