Therése Hugosson

Summary

Affiliation: Lund University
Country: Sweden

Publications

  1. doi request reprint Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7)
    Therése Hugosson
    Department of Ophthalmology, Central Hospital, Kristianstad, Sweden
    Ophthalmic Genet 30:1-6. 2009
  2. ncbi request reprint Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene
    Therése Hugosson
    Department of Clinical Sciences, Ophthalmology, Lund University, Lund, Sweden
    Arch Ophthalmol 128:772-8. 2010

Detail Information

Publications2

  1. doi request reprint Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7)
    Therése Hugosson
    Department of Ophthalmology, Central Hospital, Kristianstad, Sweden
    Ophthalmic Genet 30:1-6. 2009
    ..To characterize the clinical phenotype regarding retinal function and macular appearance in patients with spinocerebellar ataxia type 7 (SCA 7), with an emphasis on electrophysiological findings...
  2. ncbi request reprint Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene
    Therése Hugosson
    Department of Clinical Sciences, Ophthalmology, Lund University, Lund, Sweden
    Arch Ophthalmol 128:772-8. 2010
    ..To characterize the clinical phenotype, with an emphasis on electrophysiologic findings, in a family with autosomal dominant retinitis pigmentosa caused by mutation in the recently identified KLHL7 gene...