CC2D2A Mutations in Meckel and Joubert Syndromes Indicate a Genotype-Phenotype Correlation
| Auteurs | Mougou-Zerelli S, Thomas S, Szenker E, Audollent S, Elkhartoufi N, Babarit C, Romano S, Salomon R, Amiel J, Esculpavit C, Gonzales M, Escudier E, Leheup B, Loget P, Odent S, Roume J, Gerard M, Delezoide A L, Khung S, Patrier S, Cordier M P, Bouvier R, Martinovic J, Gubler M C, Boddaert N, Munnich A, Encha-Razavi F, Valente E M, Saad A, Saunier S, Vekemans M, Attie-Bitach T |
| Revue | |
| Année | 2 009 |
| Institut | I2BM |