Associated Papers
Evolutionary history of MEK1 illuminates the nature of deleterious mutations.
Andrianova EP et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
37579140 (PubMed )
Supplement: pnas.2304184120.sapp.pdf
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered.
Brinkmann J et al.
European Journal of Human Genetics : Ejhg, 2021
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