Search Results - Auber, B.

Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma by Scholz, Christian (Author) , Golas, M. M. (Author) , Weber, R. G. (Author) , Hartmann, C. (Author) , Lehmann, U. (Author) , Sahm, Felix (Author) , Schmidt, G. (Author) , Auber, B. (Author) , Sturm, M. (Author) , Schlegelberger, B. (Author) , Illig, T. (Author) , Steinemann, D. (Author) , Hofmann, W. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext