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Q34659857-EBC8E8C4-2462-4BE5-A0C6-F618A4372449
Q34659857-EBC8E8C4-2462-4BE5-A0C6-F618A4372449
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34659857-EBC8E8C4-2462-4BE5-A0C6-F618A4372449
Helicase-inactivating mutations as a basis for dominant negative phenotypes.
P2860
Q34659857-EBC8E8C4-2462-4BE5-A0C6-F618A4372449
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34659857-EBC8E8C4-2462-4BE5-A0C6-F618A4372449
rank
NormalRank
type
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Statement
wasDerivedFrom
10721265283acbfcf940a312eb56825b036408be
P2860
WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.