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Q36598570-66DE5B4B-73FC-4367-8654-0FFD279341B6
Q36598570-66DE5B4B-73FC-4367-8654-0FFD279341B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36598570-66DE5B4B-73FC-4367-8654-0FFD279341B6
Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype
P1476
Q36598570-66DE5B4B-73FC-4367-8654-0FFD279341B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36598570-66DE5B4B-73FC-4367-8654-0FFD279341B6
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
5072c4a341c3a55d7c2debe3f370f01e5035bbfe
P1476
Mutations in RIT1 cause Noonan
......
panding the clinical phenotype
@en