Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant.
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Gazzin A, et al. Among authors: villar am.
Eur J Hum Genet. 2024 Jun 1. doi: 10.1038/s41431-024-01643-6. Online ahead of print.
Eur J Hum Genet. 2024.
PMID: 38824260