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List of works by Alexandra Frohne

A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment

scientific article published on 17 November 2016

A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie disease

scientific article

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

scientific article

The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria

scientific article published on 9 November 2016

Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation

scientific article published on 18 August 2017

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