Klemens Frei
5PUBLICATIONS
21CO-AUTHORS
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Publications (5)
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|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
|Aug 20, 2017
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.Thomas Parzefall, Alexandra Frohne, Martin Koenighofer
|Jul 23, 2017
Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss.Thomas Parzefall, Alexandra Frohne, Martin Koenighofer
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Frequent Collaborators
3 joint publications
Thomas Parzefall
3 joint publications
Alexandra Frohne
3 joint publications
Christian Schoefer
3 joint publications
Franco Laccone
2 joint publications
Martin Koenighofer
2 joint publications
Juergen Neesen
1 joint publications
Elisabeth Frei
1 joint publications
Patricia Feil
1 joint publications
Trevor Lucas
1 joint publications
Hakan Cetin
