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Q26828898-2E8F5437-A5C5-49BB-B6CB-70B293BF1938
Q26828898-2E8F5437-A5C5-49BB-B6CB-70B293BF1938
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26828898-2E8F5437-A5C5-49BB-B6CB-70B293BF1938
Disease-causing missense mutations in human DNA helicase disorders
P2860
Q26828898-2E8F5437-A5C5-49BB-B6CB-70B293BF1938
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26828898-2E8F5437-A5C5-49BB-B6CB-70B293BF1938
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wasDerivedFrom
9f2cfca174dfb04e207dd3a6a1e89e59090ae509
P2860
WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.