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Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q
Stuttering is a common neurologic disorder in children that can persist into adulthood. Although stuttering displays high heritability, Mendelian segregation typically does not occur, and linkage studies have produced limited success. A genome-wide single nucleotide polymorphism (SNP) linkage scan i...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2011
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3474244/ https://ncbi.nlm.nih.gov/pubmed/22205390 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-011-1134-2 |
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