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

Cristina Has, Vesarat Wessagowit, Monica Pascucci, Corinna Baer, Biagio Didona, Christian Wilhelm, Cristina Pedicelli, Andrea Locatelli, Jürgen Kohlhase, Gabrielle H.S. Ashton, Gianluca Tadini, Giovanna Zambruno, Leena Bruckner-Tuderman, John A. McGrath, Daniele Castiglia

Research output: Contribution to journal › Article › peer-review

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