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Q33715782-D5BA4199-9F36-48B1-A523-A75DD7E9A420
Q33715782-D5BA4199-9F36-48B1-A523-A75DD7E9A420
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Statement
http://www.wikidata.org/entity/statement/Q33715782-D5BA4199-9F36-48B1-A523-A75DD7E9A420
Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports.
P2860
Q33715782-D5BA4199-9F36-48B1-A523-A75DD7E9A420
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33715782-D5BA4199-9F36-48B1-A523-A75DD7E9A420
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wasDerivedFrom
166da0bd20f4c4d875a0ed0c9b38e025b494ed37
P2860
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.