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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
Authors: Laumonnier, Frédéric; Bonnet-Brilhault, Frédérique; Gomot, Marie; Blanc, Romuald; David, Albert; Moizard, Marie-Pierre; Raynaud, Martine; Ronce, Nathalie; Lemonnier, Eric; Calvas, Patrick; Laudier, Béatrice; Chelly, Jamel; Fryns, Jean-Pierre; Ropers, Hans-Hilger; Hamel, Ben C. J.; Andres, Christian; Barthélémy, Catherine; Moraine, Claude; Briault, Sylvain
Date of Publication (YYYY-MM-DD): 2004-02-12
Title of Journal: American Journal of Human Genetics
Volume: 74
Issue / Number: 3
Start Page: 552
End Page: 557
Document Type: Article
ID: 224730.0
MECP2 gene mutations in non-syndromic X-linked mental retardation: Phenotype-genotype correlation
Authors: Gomot, Marie; Gendrot, Chantal; Verloes, Alain; Raynaud, Martine; David, Albert; Yntema, Helger G.; Dessay, Sabine; Kalscheuer, Vera; Frints, Suzanne; Convert, Philippe; Briault, Sylvain; Blesson, Sophie; Toutain, Annick; Chelly, Jamel; Desportes, Vincent; Moraine, Claude
Date of Publication (YYYY-MM-DD): 2003-12-01
Title of Journal: American Journal of Medical Genetics Part A
Volume: 123A
Issue / Number: 2
Start Page: 129
End Page: 139
Document Type: Article
ID: 127597.0
Entries: 1-2  
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