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Q36598570-06876F92-152E-4EE5-9D4D-28F8A09473E3
Q36598570-06876F92-152E-4EE5-9D4D-28F8A09473E3
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http://www.wikidata.org/entity/statement/Q36598570-06876F92-152E-4EE5-9D4D-28F8A09473E3
Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype
P1433
Q36598570-06876F92-152E-4EE5-9D4D-28F8A09473E3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36598570-06876F92-152E-4EE5-9D4D-28F8A09473E3
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5072c4a341c3a55d7c2debe3f370f01e5035bbfe
P1433
Clinical Genetics