| Affiliation auteurs | !!!! Error affiliation !!!! |
| Titre | De novo mutations in protein kinase genes CAMK2A and CAMK2B cause intellectual disability |
| Type de publication | Journal Article |
| Year of Publication | 2019 |
| Auteurs | Kury S., van Woerden G.M, Besnard T., Latypova X., Cho M.T, Sanders S., Stessman H.AF, Sellars E.A, Berg J., Waugh J.L, Robak L.A, Bernstein J.A, Deardorff M., Hoganson G.E, Johnson D.S, Dabir T., Sarkar A., Lesca G., Terhal P.A, Prescott T.E, Grange D.K, van Haeringen A., Lam C., Mirzaa G., Helbig K.L, Afenjar A., Nava C., Vitobello A., Faivre L., Cogne B., Rosenfeld J.A, Agrawal P.B, Odent S., Bezieau S., Elgersma Y., Mercier S., Consortium CAMK2AB |
| Journal | EUROPEAN JOURNAL OF HUMAN GENETICS |
| Volume | 27 |
| Pagination | 837-838 |
| Date Published | JUL |
| Type of Article | Meeting Abstract |
| ISSN | 1018-4813 |
