Federico Santoni
0000-0002-3258-4747
CHUV
3 papers found
Refreshing results…
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2
Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts.
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