APA

Hébert B., Pietropaolo S., Même S., Laudier B., Laugeray A., Doisne N., Quartier A., Lefeuvre S., Got L., Cahard D., Laumonnier F., Crusio W. E., Pichon J., Menuet A., Perche O. & Briault S. (20150330). Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule. : Orphanet journal of rare diseases.

Chicago

Hébert Betty, Pietropaolo Susanna, Même Sandra, Laudier Béatrice, Laugeray Anthony, Doisne Nicolas, Quartier Angélique, Lefeuvre Sandrine, Got Laurence, Cahard Dominique, Laumonnier Frédéric, Crusio Wim E, Pichon Jacques, Menuet Arnaud, Perche Olivier and Briault Sylvain. 20150330. Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule. : Orphanet journal of rare diseases.

Harvard

Hébert B., Pietropaolo S., Même S., Laudier B., Laugeray A., Doisne N., Quartier A., Lefeuvre S., Got L., Cahard D., Laumonnier F., Crusio W. E., Pichon J., Menuet A., Perche O. and Briault S. (20150330). Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule. : Orphanet journal of rare diseases.

MLA

Hébert Betty, Pietropaolo Susanna, Même Sandra, Laudier Béatrice, Laugeray Anthony, Doisne Nicolas, Quartier Angélique, Lefeuvre Sandrine, Got Laurence, Cahard Dominique, Laumonnier Frédéric, Crusio Wim E, Pichon Jacques, Menuet Arnaud, Perche Olivier and Briault Sylvain. Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule. : Orphanet journal of rare diseases. 20150330.