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Q34556666-FCCB2219-E18A-472E-BF6D-21023860F4FF
Q34556666-FCCB2219-E18A-472E-BF6D-21023860F4FF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34556666-FCCB2219-E18A-472E-BF6D-21023860F4FF
Dominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis".
P2860
Q34556666-FCCB2219-E18A-472E-BF6D-21023860F4FF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34556666-FCCB2219-E18A-472E-BF6D-21023860F4FF
rank
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type
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wasDerivedFrom
f4971b31d0eacdd046a23b1b6bec4658202c3094
P2860
Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype