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

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TitleVariants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications
DateJanuary 1st, 2021
Issue nameEuropean Journal of Human Genetics
Issue numberv29.1 p51-60
DOI10.1038/s41431-020-00708-6
AuthorsLissewski C, Chune V, Pantaleoni F, De Luca A, Capri Y, Brinkmann J, Lepri F, Daniele P, Leenders E, Mazzanti L, Scarano E, Radio FC, Kutsche K, Kuechler A, Gérard M, Ranguin K, Legendre M, Vial Y, van der Burgt I, Rinne T, Andreucci E, Mastromoro G, Digilio MC, Cave H, Tartaglia M & Zenker M
MTGsMTG5
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