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Q34695879-0990F54C-ED4B-4853-803E-BA2047B46996
Q34695879-0990F54C-ED4B-4853-803E-BA2047B46996
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34695879-0990F54C-ED4B-4853-803E-BA2047B46996
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.
P2860
Q34695879-0990F54C-ED4B-4853-803E-BA2047B46996
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34695879-0990F54C-ED4B-4853-803E-BA2047B46996
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wasDerivedFrom
16696fdc913339d228425ba4615a2dab2d42a1c8
P2860
Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa.