Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation

Carina Frykholm, Joakim Klar, Hanna Arnesson, Anna-Carin Rehnman, Marianne Lodahl, Ulla Wedén, Niklas Dahl, Lisbeth Tranebjærg, Nanna D Rendtorff

5 Citationer (Scopus)

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology

Neuroscience

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