Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy

@inproceedings{Rosenberg2010ClinicalAG,
  title={Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy},
  author={Thomas Rosenberg and Ben R. Roos and Thorkild Johnsen and Niels Bech and Todd E. Scheetz and Michael Larsen and Edwin M. Stone and John H. Fingert},
  booktitle={Molecular vision},
  year={2010}
}
PURPOSE To describe the phenotype of a family with an autosomal dominant macular dystrophy and identify the chromosomal location of the gene that causes this phenotype. METHODS Twelve members of a three-generation family underwent routine clinical examination, including fundus photography. Four of the patients underwent extended examination with Goldmann perimetry, full-field electroretinogram, dark adaptation, and color vision testing, and two patients underwent optical coherence tomography… CONTINUE READING

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