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Q35568316-78855B2B-EFE1-481C-AD74-9C03F1A81C67
Q35568316-78855B2B-EFE1-481C-AD74-9C03F1A81C67
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Statement
http://www.wikidata.org/entity/statement/Q35568316-78855B2B-EFE1-481C-AD74-9C03F1A81C67
Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease.
P2860
Q35568316-78855B2B-EFE1-481C-AD74-9C03F1A81C67
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35568316-78855B2B-EFE1-481C-AD74-9C03F1A81C67
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wasDerivedFrom
df8b467180aca7a57df450fc1ae972863f29a2b3
P2860
Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein