Stefan F Nemec
1PUBLICATIONS
16CO-AUTHORS
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Publications (1)
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|Nov 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation.Alexandra Frohne, Martin Koenighofer, Hakan Cetin
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Frequent Collaborators
1 joint publications
Alexandra Frohne
1 joint publications
Martin Koenighofer
1 joint publications
Hakan Cetin
1 joint publications
Michael Nieratschker
1 joint publications
David T Liu
1 joint publications
Franco Laccone
1 joint publications
Juergen Neesen
1 joint publications
Ursula Schwarz-Nemec
1 joint publications
Christian Schoefer
1 joint publications
Karen B Avraham
