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Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, et al.Mitochondrion|September 28, 2011
Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distributionA M Voets, B J C van den Bosch, A P Stassen, et al.Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.Human Molecular Genetics|August 7, 2001
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1FK N Alagramam, H Yuan, M H Kuehn, et al.Genome Medicine|December 31, 2024
Interpretation and classification of FBN1 variants associated with Marfan syndrome: consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panelA Drackley, C Somerville, P Arnaud, et al.Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.Pageof 5