Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.
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J. McGrath | C. Has | G. Zambruno | C. Pedicelli | J. Kohlhase | L. Bruckner-Tuderman | V. Wessagowit | C. Wilhelm | D. Castiglia | B. Didona | G. Tadini | M. Pascucci | G. Ashton | A. Locatelli | Corinna Baer