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Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.

机译：通过全外显子组测序的分子研究揭示了突然意外死亡综合征的泰国受害者中的高比例致病变异。

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Bhoom Suktitipat; Sakda Sathirareuangchai; Ekkapong Roothumnong; Wanna Thongnoppakhun; Purin Wangkiratikant; Nutchavadee Vorasan; Rungroj Krittayaphong; Manop Pithukpakorn; Warangkna Boonyapisit;
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1. Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death [J] . Lopez Hector U., Haverfield Eden, Chung Wendy K. Pediatric and developmental pathology: the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society . 2015,第4期

机译：全基因组测序发现意外婴儿死亡案例中的CLCNKB突变
2. Whole Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death [J] . Cutz Ernest Pediatric and developmental pathology: the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society . 2015,第4期

机译：整个外显子组测序揭示了意外婴儿死亡案例中的CLCNKB突变
3. Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes [J] . Neubauer Jacqueline, Lecca Maria Rita, Russo Giancarlo, International journal of legal medicine . 2018,第4期

机译：在34例突然未解释的死亡（SUD）受害者中的exome分析主要鉴定了通道病相关基因的变体
4. Whole Exome Sequencing Approach to Identify Genetic Variants Causing Sudden Unexplained Death Syndrome [C] . Seok-Hwee Koo, Paul Chui, Chee Seng Ku, Molecular Medicine TRI-CON. . 2014

机译：识别遗传变异突然未解释的死亡综合征的整体exome测序方法
5. Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome [O] . Bhoom Suktitipat, Sakda Sathirareuangchai, Ekkapong Roothumnong, 2011

机译：通过全外显子组测序进行的分子调查显示，泰国突发性意外死亡综合征受害者中有很大比例的致病变异
6. Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases [O] . Elias L. Salfati, Emily G. Spencer, Sarah E. Topol, 2019

机译：重新分析全外膜测序数据，揭示了新型诊断变体，提高了猝死和特发性疾病的分子诊断产率
7. Guidelines for Death Scene Investigation of Sudden, Unexplained Infant Deaths:211 Recommendations of the Interagency Panel on Sudden Infant Death Syndrome. 211 Morbidity and Mortality Weekly Report, Vol. 45, No. RR-10, June 21, 1996 [R] . Iyasu, S., Rowley, D. L., Hanzlick, R. L., 1996

机译：关于突发，原因不明的婴儿死亡的死亡现场调查指南：211关于突发婴儿死亡综合症的机构间小组的建议。 211发病率和死亡率周报，第一卷。 45，第RR-10号，1996年6月21日

Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.

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