Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

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BONNET, C., GRATI, M., MARLIN, S., LEVILLIERS, J., HARDELIN, J. P., PARODI, M., NIASME-GRARE, M., ZELENIKA, D., DELEPINE, M., FELDMANN, D., JONARD, L., EL-AMRAOUI, A., WEIL, D., DELOBEL, B., VINCENT, C., DOLLFUS, Helene, ELIOT, M. M., DAVID, A., CALAIS, C., VIGNERON, J., MONTAUT-VERIENT, B., BONNEAU, D., DUBIN, J., THAUVIN, C., DUVILLARD, A., FRANCANNET, C., MOM, T., LACOMBE, D., DURIEZ, F., DROUIN-GARRAUD, V., THUILLIER-OBSTOY, M. F., SIGAUDY, S., FRANCES, A. M., COLLIGNON, P., CHALLE, G., COUDERC, R., LATHROP, M., SAHEL, J. A., WEISSENBACH, J., PETIT, C. et DENOYELLE, F., 2011. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet Journal of Rare Diseases [en ligne]. 11 mai 2011. Vol. 6. [Consultésans date]. DOI 10.1186/1750-1172-6-21. Consulté de : https://ojrd.biomedcentral.com/articles/10.1186/1750-1172-6-211. .