Marcus Müller

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2020
Publications (10 Years): 1

Top Topics

Genome Wide Analysis

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Aboulfazl Rad, Thore Schade-Mann, Philipp Gamerdinger, Grigoriy A Yanus, Björn Schulte, Marcus Müller, Evgeny N Imyanitov, Saskia Biskup, Hubert Löwenheim, Anke Tropitzsch, Barbara Vona
Aberrant COL11A1 splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus. Human mutation 42 (1) (2020)