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Q28731691-7DD07EA8-399B-4C35-8B45-FB254D860331
Q28731691-7DD07EA8-399B-4C35-8B45-FB254D860331
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28731691-7DD07EA8-399B-4C35-8B45-FB254D860331
CNTF and retina
P2860
Q28731691-7DD07EA8-399B-4C35-8B45-FB254D860331
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28731691-7DD07EA8-399B-4C35-8B45-FB254D860331
rank
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type
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wasDerivedFrom
8e3bfc3412aec9d94dde938c1571338ae9990d7f
P2860
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14.