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Q37293265-EFA8E85F-414E-4670-96C7-EE5283FFD7A6
Q37293265-EFA8E85F-414E-4670-96C7-EE5283FFD7A6
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Statement
http://www.wikidata.org/entity/statement/Q37293265-EFA8E85F-414E-4670-96C7-EE5283FFD7A6
Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families.
P2860
Q37293265-EFA8E85F-414E-4670-96C7-EE5283FFD7A6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37293265-EFA8E85F-414E-4670-96C7-EE5283FFD7A6
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wasDerivedFrom
ca98186f2b9cf4acc997991be52b304a23a5a7dd
P2860
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.