Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland

L Huopaniemi, A Rantala, H Forsius, M Somer, A de la Chapelle, T Alitalo

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume7
Pages (from-to)368-376
Number of pages9
ISSN1018-4813
Publication statusPublished - 1999
MoE publication typeA1 Journal article-refereed

Fields of Science

  • X-chromosome
  • retinoschisis
  • mutation screening
  • haplotypes
  • LINKAGE DISEQUILIBRIUM
  • REFINED LOCALIZATION
  • YAC CONTIG
  • GENE
  • POPULATIONS
  • DNA
  • MAP
  • AGE
  • RS
  • 118 Biological sciences

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