Laurent Fasano

Years Active: 2022-2022
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Irene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, Ahmed Fatmi, Fabrice Richard, Thien Phong Vu Manh, Andrew J Saurin, Guylène Feuillet, Colette Denis, Adrian S Woolf, Joost P Schanstra, Petra Zürbig, Xavier Caubit, Laurent Fasano
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects. Human molecular genetics 31 (12) (2022)
Xavier Caubit, Paolo Gubellini, Pierre L Roubertoux, Michèle Carlier, Jordan Molitor, Dorian Chabbert, Mehdi Metwaly, Pascal Salin, Ahmed Fatmi, Yasmine Belaidouni, Lucie Brosse, Lydia Kerkerian-Le Goff, Laurent Fasano
Correction: Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors. Translational psychiatry 12 (1) (2022)
Xavier Caubit, Paolo Gubellini, Pierre L Roubertoux, Michèle Carlier, Jordan Molitor, Dorian Chabbert, Mehdi Metwaly, Pascal Salin, Ahmed Fatmi, Yasmine Belaidouni, Lucie Brosse, Lydia Kerkerian-Le Goff, Laurent Fasano
Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors. Translational psychiatry 12 (1) (2022)

Laurent Fasano.css-eqlu8i{font-size:small;padding-left:4px;}