Novel high-throughput SNP genotyping cosegregation analysis for genetic diagnosis of autosomal recessive retinitis pigmentosa and Leber congenital amaurosis

  1. Pomares, E.
  2. Marfany, G.
  3. Brión, Ma.J.
  4. Carracedo, A.
  5. Gonzàlez-Duarte, R.
Journal:
Human Mutation

ISSN: 1059-7794

Year of publication: 2007

Volume: 28

Issue: 5

Pages: 511-516

Type: Article

DOI: 10.1002/HUMU.20479 GOOGLE SCHOLAR
Data source: Scopus