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Q33909665-664A41A4-4D42-461E-8880-2CE8EE80196B
Q33909665-664A41A4-4D42-461E-8880-2CE8EE80196B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33909665-664A41A4-4D42-461E-8880-2CE8EE80196B
Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway.
P2860
Q33909665-664A41A4-4D42-461E-8880-2CE8EE80196B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33909665-664A41A4-4D42-461E-8880-2CE8EE80196B
rank
NormalRank
type
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Statement
wasDerivedFrom
78d073c4194b6a06775699423888e967b47cb70b
P2860
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL