Skip to Main Content

Paper Details

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV.
Hum Mutat
19
2021
ARSG, Arylsulfatase, Arylsulfatase G enzyme, Arylsulfatase G gene, Usher syndrome, Usher syndrome type IV, canine, deaf-blindness syndrome, humans, lysosomal storage disorder, murine, retinitis pigmentosa, sensorineural hearing loss, sulfatase, visual and auditory impairment
Author NameAffiliation
Mathieu QuinodozInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Mathieu QuinodozUniversity of Basel
Mathieu QuinodozUniversity of Leicester
Carlo RivoltaInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Carlo RivoltaUniversity of Basel
Carlo RivoltaUniversity of Leicester
Carlo RivoltaInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Carlo RivoltaUniversity of Basel
Carlo RivoltaUniversity of Leicester
  • 1 - 9

Datasets