Specific reading disability: identification of an inherited form through linkage analysis

Science. 1983 Mar 18;219(4590):1345-7. doi: 10.1126/science.6828864.

Abstract

Linkage analysis in families with apparent autosomal dominant reading disability produced a lod score of 3.241. Since the traditionally accepted significance level for linkage is a lod score of 3.0, these results strongly suggest that a gene playing a major etiologic role in one form of reading disability is on chromosome 15.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosomes, Human, 13-15*
  • Dyslexia / genetics*
  • Genetic Linkage
  • Humans
  • Pedigree