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Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome

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Description scientific article published on 19 June 2015
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author: Xiaoxu Yang  Yuehua Zhang  Qixi Wu  August Y Huang  Adam Yongxin Ye 

Publication date June 19, 2015
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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034833

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