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Q36598570-E4D4E9A2-A0F1-4E7C-88AA-46E21D5AE3A2
Q36598570-E4D4E9A2-A0F1-4E7C-88AA-46E21D5AE3A2
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http://www.wikidata.org/entity/statement/Q36598570-E4D4E9A2-A0F1-4E7C-88AA-46E21D5AE3A2
Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype
P2860
Q36598570-E4D4E9A2-A0F1-4E7C-88AA-46E21D5AE3A2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36598570-E4D4E9A2-A0F1-4E7C-88AA-46E21D5AE3A2
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a7fef89deb7ebe94c7588276484aaa13fd80b219
P2860
Contribution of RIT1 mutations to the pathogenesis of Noonan syndrome: four new cases and further evidence of heterogeneity