Associated Papers
Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.
Schubert S et al.
Molecular and Cellular Probes, 2015
Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?
Javaher P et al.
Fertility and Sterility, 2012
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility.
Vinci G et al.
Fertility and Sterility, 2009
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