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Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33.

Authors :
Raza, Muhammad Hashim
Riazuddin, Sheikh
Drayna, Dennis
Source :
Human Genetics. Oct2010, Vol. 128 Issue 4, p461-463. 3p. 1 Diagram, 1 Chart.
Publication Year :
2010

Abstract

Stuttering is a common speech disorder with substantial genetic contributions. To better understand the genetic factors involved in stuttering, we performed a genome-wide linkage study in a newly-ascertained consanguineous stuttering family from Pakistan. A linkage scan in this family using parametric linkage analysis revealed significant linkage only on chromosome 3q13.2–3q13.33, with a maximum two-point LOD score of 4.23 under an autosomal recessive model of inheritance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03406717
Volume :
128
Issue :
4
Database :
Academic Search Index
Journal :
Human Genetics
Publication Type :
Academic Journal
Accession number :
53555928
Full Text :
https://doi.org/10.1007/s00439-010-0871-y