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Q24295035-01B31305-71BB-4E81-86D9-BDD10540FC91
Q24295035-01B31305-71BB-4E81-86D9-BDD10540FC91
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http://www.wikidata.org/entity/statement/Q24295035-01B31305-71BB-4E81-86D9-BDD10540FC91
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis
P2860
Q24295035-01B31305-71BB-4E81-86D9-BDD10540FC91
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24295035-01B31305-71BB-4E81-86D9-BDD10540FC91
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wasDerivedFrom
0663dbce09784a17175ddf0c121e4ad40fb9a323
P2860
NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway