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Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33.
- 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]
- Subjects :
- *CELL nuclei
*LOCUS (Genetics)
*GENETICS
*SPEECH disorders
Subjects
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