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Q23815226-0FCB207C-D64A-45E1-BE92-6224B4FAAF87
Q23815226-0FCB207C-D64A-45E1-BE92-6224B4FAAF87
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Statement
http://www.wikidata.org/entity/statement/Q23815226-0FCB207C-D64A-45E1-BE92-6224B4FAAF87
Improved exome prioritization of disease genes through cross-species phenotype comparison
P2860
Q23815226-0FCB207C-D64A-45E1-BE92-6224B4FAAF87
BestRank
Statement
http://www.wikidata.org/entity/statement/Q23815226-0FCB207C-D64A-45E1-BE92-6224B4FAAF87
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wasDerivedFrom
a62734c9acad973cd811923cd75f018241aa462d
P2860
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome