Dr. Nicola Gloeckle joined CeGaT in April 2011 to strengthen the Molecular Diagnostics facility. She leads the Hereditary Eye Disease Panel diagnostic team

Nicola gained her scientific qualification by studying biology, particularly in the department of human genetics, and by graduating from the Clinic of Medical Genetics, University of Tuebingen. Her main focus is the search for mutations and sequence variants for neurological disorders (Mov Disord. 2010), to which the different forms of dystonia belong to as well. Within her research work in the field of dystonia, Nicola Gloeckle became conversant with all methods of mutation analysis.

nicola.gloeckle {at} cegat.de