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Q38681476-222F5620-AAFB-4B1B-BB30-ED0268EBA7E4
Q38681476-222F5620-AAFB-4B1B-BB30-ED0268EBA7E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38681476-222F5620-AAFB-4B1B-BB30-ED0268EBA7E4
Expanding the mutation and clinical spectrum of Roberts syndrome.
P2860
Q38681476-222F5620-AAFB-4B1B-BB30-ED0268EBA7E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38681476-222F5620-AAFB-4B1B-BB30-ED0268EBA7E4
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Statement
wasDerivedFrom
7884bc0bc8e368171e7cfafd3ba6f13ec3b6c427
P2860
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.