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Q36458923-21E4A35B-A08C-4F4F-A98C-DFD9CBD9A3AA
Q36458923-21E4A35B-A08C-4F4F-A98C-DFD9CBD9A3AA
BestRank
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http://www.wikidata.org/entity/statement/Q36458923-21E4A35B-A08C-4F4F-A98C-DFD9CBD9A3AA
A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophy.
P2860
Q36458923-21E4A35B-A08C-4F4F-A98C-DFD9CBD9A3AA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36458923-21E4A35B-A08C-4F4F-A98C-DFD9CBD9A3AA
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wasDerivedFrom
9948ea902cbedf7efc1fb89f759d0eb2864fc05e
P2860
Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy