Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype
Titel:
Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype
Auteur:
Grosch, Melanie Grüner, Barbara Spranger, Stephanie Stütz, Adrian M. Rausch, Tobias Korbel, Jan O. Seelow, Dominik Nürnberg, Peter Sticht, Heinrich Lausch, Ekkehart Zabel, Bernhard Winterpacht, Andreas Tagariello, Andreas