Characterization of a mutation commonly associated with persistent stuttering : evidence for a founder mutation
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概要
- 論文の詳細を見る
- 2011-01-01
著者
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Drayna Dennis
National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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Kang Changsoo
National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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FEDYNA Alison
National Institute on Deafness and Other Communication Disorders, National Institutes of Health
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Fedyna Alison
National Institute On Deafness And Other Communication Disorders National Institutes Of Health
関連論文
- Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation
- THE SEARCH FOR THE WERNER SYNDROME GENE
- Evaluation of the association between polymorphisms at the DRD2 locus and stuttering
- Characterization of a mutation commonly associated with persistent stuttering : evidence for a founder mutation