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Q38076196-03481C7E-662A-4C7C-B3EB-ED95165B2F83
Q38076196-03481C7E-662A-4C7C-B3EB-ED95165B2F83
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38076196-03481C7E-662A-4C7C-B3EB-ED95165B2F83
Autosomal dominant retinitis pigmentosa secondary to pre-mRNA splicing-factor gene PRPF31 (RP11): review of disease mechanism and report of a family with a novel 3-base pair insertion.
P2860
Q38076196-03481C7E-662A-4C7C-B3EB-ED95165B2F83
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38076196-03481C7E-662A-4C7C-B3EB-ED95165B2F83
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type
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Statement
wasDerivedFrom
a66c8ca9ca20cac613af4aec69fc1b573f89a857
P2860
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.