![]() ![]() To reach this goal, we include families from Pakistan and Turkey via collaborations with researchers in these countries. The aim of our studies is to identify genetic defects that underlie hereditary hearing impairment in the Netherlands and to unravel the molecular pathogenesis. Although more than 60 deafness genes are known already, it is estimated that more than hundred additional genes await identification. Dominant, recessive, X-linked, Y-linked and mitochondrial inheritance patterns can be seen. We largely concentrate on the genetics of nonsyndromic deafness. Clinical and genetic heterogeneity of hearing impairment is enormous. Hereditary hearing impairment (or deafness) is among the most common monogenic disorders but can also be multifactorial as is the case for age-related hearing loss. Hereditary hearing impairment (or deafness) Netherlands Institute for Neuroscience (NIN). ![]() Western University Ontario, Brain & Mind Institute.Monash Institute of Cognitive and Clinical Neurosciences.Brain Mind Institute of the Ecole Polytechnique Fédérale de Lausanne (EPFL) Brain Mind Institute of the Ecole Polytechnique Fédérale de Lausanne (EPFL).Preferred Institutional Partners Preferred Institutional Partners.DSS Best Practices for Conference Organization.Diversity and Sustainable Science Diversity and Sustainable Science.Diversity and Sustainable Science Committee.Summer School Stress & Cognition Summer School Stress & Cognition.Former Donders Lectures Former Donders Lectures.Postdoctoral researchers Postdoctoral researchers. ![]()
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