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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Veröffentlicht in:	Human genetics 2012-02, Vol.131 (2), p.311-313
Hauptverfasser:	Raza, Muhammad Hashim, Amjad, Rana, Riazuddin, Sheikh, Drayna, Dennis
Format:	Artikel
Sprache:	eng
Schlagworte:	Biomedical and Life Sciences Biomedicine Chromosomes Chromosomes, Human, Pair 16 Consanguinity Female Gene Function Genetic Linkage Genomes Haplotypes Human Genetics Humans Male Metabolic Diseases Molecular biology Molecular Medicine Pedigree Short Report Stuttering Stuttering - genetics
Online-Zugang:	Volltext
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