Data di Pubblicazione:
2006
Abstract:
R-spondins are a recently characterized small family of growth factors. Here we show that human R-spondin1 (RSPO1) is the gene disrupted in a recessive syndrome characterized by XX sex reversal, palmoplantar hyperkeratosis and predisposition to squamous cell carcinoma of the skin. Our data show, for the first time, that disruption of a single gene can lead to complete female-to-male sex reversal in the absence of the testis determining gene, SRY.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
R-spondin1; sex determination; skin differentiation
Elenco autori:
P., Parma; O., Radi; V., Vidal; Chaboissier, M. C.; E., Dellambra; S., Valentini; L., Guerral; A., Schedl; Camerino, Giovanna
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