The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered

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TitleThe clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered
DateMarch 1st, 2021
Issue nameEuropean Journal of Human Genetics
Issue numberv29.3 p524-527
DOI10.1038/s41431-020-00743-3
AuthorsBrinkmann J, Lissewski C, Pinna V, Vial Y, Pantaleoni F, Lepri F, Daniele P, Burnyte B, Cuturilo G, Fauth C, Gezdirici A, Kotzot D, Güleç EY, Iotova V, Schanze D, Ramond F, Havlovicová M, Utine GE, Simsek-Kiper PO, Stoyanova M, Verloes A, De Luca A, Tartaglia M, Cavé H & Zenker M
MTGsMTG5
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