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Publication | Open Access

Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications

DOIFull Paper Access

31

Citations

16

References

2020

Year

Valérie Chune, Francesca Pantaleoni, Alessandro De Luca, Yline Capri, Julia Brinkmann, Francesca Romana Lepri, Paola Daniele, Erika Leenders, Laura Mazzanti, Emanuela Scarano,
European Journal of Human Genetics

References

YearCitations

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