Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.

MLA

Has, Cristina, et al. “Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene.” The Journal of Investigative Dermatology, vol. 126, no. 8, Aug. 2006, pp. 1776–83. EBSCOhost, https://doi.org/10.1038/sj.jid.5700339.

APA

Has, C., Wessagowit, V., Pascucci, M., Baer, C., Didona, B., Wilhelm, C., Pedicelli, C., Locatelli, A., Kohlhase, J., Ashton, G. H. S., Tadini, G., Zambruno, G., Bruckner-Tuderman, L., McGrath, J. A., & Castiglia, D. (2006). Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene. The Journal of Investigative Dermatology, 126(8), 1776–1783. https://doi.org/10.1038/sj.jid.5700339

Chicago

Has, Cristina, Vesarat Wessagowit, Monica Pascucci, Corinna Baer, Biagio Didona, Christian Wilhelm, Cristina Pedicelli, et al. 2006. “Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene.” The Journal of Investigative Dermatology 126 (8): 1776–83. doi:10.1038/sj.jid.5700339.