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Q34556666-D49B2234-A121-47F8-B879-03D3DC0B5F5B
Q34556666-D49B2234-A121-47F8-B879-03D3DC0B5F5B
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http://www.wikidata.org/entity/statement/Q34556666-D49B2234-A121-47F8-B879-03D3DC0B5F5B
Dominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis".
P2860
Q34556666-D49B2234-A121-47F8-B879-03D3DC0B5F5B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34556666-D49B2234-A121-47F8-B879-03D3DC0B5F5B
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wasDerivedFrom
f4971b31d0eacdd046a23b1b6bec4658202c3094
P2860
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.