Concepedia

Publication | Open Access

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

DOIFull Paper Access

80

Citations

45

References

2019

Year

Yline Capri, Elisabetta Flex, Oliver H.F. Krumbach, Giovanna Carpentieri, Serena Cecchetti, Christina Lißewski, Soheila Rezaei Adariani, Denny Schanze, Julia Brinkmann, Juliette Piard,
The American Journal of Human Genetics

References

YearCitations

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