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Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33
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 parametr...
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Main Authors: | , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2010
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3030966/ https://ncbi.nlm.nih.gov/pubmed/20706738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-010-0871-y |
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