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Q35591946-08D588D6-D391-41C9-9FB8-0EA7EFD4887F
Q35591946-08D588D6-D391-41C9-9FB8-0EA7EFD4887F
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http://www.wikidata.org/entity/statement/Q35591946-08D588D6-D391-41C9-9FB8-0EA7EFD4887F
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene.
P2860
Q35591946-08D588D6-D391-41C9-9FB8-0EA7EFD4887F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35591946-08D588D6-D391-41C9-9FB8-0EA7EFD4887F
rank
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type
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Statement
wasDerivedFrom
8c7881121a8e5bd29a812f76f44f15b7611bcbc6
P2860
Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families.