Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.
Hum Genet
; 128(4): 461-3, 2010 Oct.
Article
en En
| MEDLINE
| ID: mdl-20706738
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.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Tartamudeo
/
Cromosomas Humanos Par 3
/
Estudio de Asociación del Genoma Completo
/
Genes Recesivos
Tipo de estudio:
Diagnostic_studies
/
Prognostic_studies
Límite:
Female
/
Humans
/
Male
País/Región como asunto:
Asia
Idioma:
En
Revista:
Hum Genet
Año:
2010
Tipo del documento:
Article
País de afiliación:
Estados Unidos