Vigdis Brox

Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II

Bo Dreyer, Vigdis Brox, Lisbeth Tranebjærg et al. · Human Mutation · 2008 · 107 citations

A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation

Bo Dreyer, Lisbeth Tranebjærg, Vigdis Brox et al. · The American Journal of Human Genetics · 2001 · 80 citations · Full text

Widespread 2299Delg, Medicine, Genetics +9

Fukutin-Related Protein Resides in the Golgi Cisternae of Skeletal Muscle Fibres and Forms Disulfide-Linked Homodimers via an N-Terminal Interaction

M. Alhamidi, Elisabeth Kjeldsen Buvang, Toril Fagerheim et al. · PLoS ONE · 2011 · 39 citations · Full text

Protein Secretion, Forms Disulfide-linked Homodimers, Molecular Biology +28

Limb girdle muscular dystrophy type 2I: No correlation between clinical severity, histopathology and glycosylated α-dystroglycan levels in patients homozygous for common FKRP mutation

M. Alhamidi, Vigdis Brox, Eva Stensland et al. · Neuromuscular Disorders · 2017 · 35 citations · Full text

Urology, Medicine, Common Fkrp Mutation +6

Human cytomegalovirus (HCMV) and hearing impairment: Infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49—Both involved in dominantly inherited, sensorineural, hearing impairment

Mona Nystad, Toril Fagerheim, Vigdis Brox et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 2007 · 33 citations · Full text

Loci Dfna7, Audiology, Immunology +8