A Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation

This publication has 11 references indexed in Scilit:

• Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa
  Science, 1998
• Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
  Nature Genetics, 1997
• Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
  Nature Genetics, 1997
• The prevalence of Usher syndrome and other retinal dystrophy‐hearing impairment associations
  Clinical Genetics, 1997
• Usher syndrome in the city of Birmingham---prevalence and clinical classification
  British Journal of Ophthalmology, 1997
• Usher's syndrome type 3 in Finland
  The Laryngoscope, 1995
• Defective myosin VIIA gene responsible for Usher syndrome type IB
  Nature, 1995
• Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q
  Human Molecular Genetics, 1995
• Phenotypic diversity, allelic series and modifier genes
  Nature Genetics, 1994
• Clinical diagnosis of the Usher syndromes
  American Journal of Medical Genetics, 1994