Christian Schöfer

7PUBLICATIONS
37CO-AUTHORS
Nutrigenomics and personalised nutritionGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsStructural properties of condensed matterGene mapping
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Publications (7)

|Feb 24, 2024
Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria.

Alexandra Frohne, Sybille Vrabel, Franco Laccone

|Nov 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation.

Alexandra Frohne, Martin Koenighofer, Hakan Cetin

|Apr 14, 2021
Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma.

Martin Koenighofer, Thomas Parzefall, Alexandra Frohne

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