Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech

被引：0
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作者：
Elizabeth A Worthey
Gordana Raca
Jennifer J Laffin
Brandon M Wilk
Jeremy M Harris
Kathy J Jakielski
David P Dimmock
Edythe A Strand
Lawrence D Shriberg
机构：
[1] Medical College of Wisconsin,Department of Pediatrics
[2] Medical College of Wisconsin,Human and Molecular Genetics Center
[3] University of Chicago Medical Center,Cancer Cytogenetics Laboratory
[4] Wisconsin State Laboratory of Hygiene Clinical Genetics Laboratories,Communication Sciences and Disorders
[5] Augustana College,Department of Neurology
[6] Mayo Clinic,Waisman Center
[7] University of Wisconsin–Madison,undefined
来源：
Journal of Neurodevelopmental Disorders | 2013年 / 5卷
关键词：
Apraxia of speech; Developmental verbal dyspraxia; Next-generation sequencing; Speech disorder; Whole-exome sequencing;
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