Functional significance of channelopathy gene variants in unexplained death

Author:

Gando Ivan,Yang Hua-Qian,Coetzee William A.ORCID

Funder

National Institute of Justice

American SIDS Institute

Seventh Masonic District Association, Inc.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Pathology and Forensic Medicine

Reference57 articles.

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2. Centers for Disease Control and Prevention. Prevention CfDCa. CDC Grand Rounds: Public health approaches to reducing U.S. infant mortality. http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6231a3.htm . Accessed 19 Nov 2018.

3. Murphy S, Xu JQ, Kochanek KD. Deaths: preliminary data for 2010. Natl Vital Stat Rep. 2012;60(4) http://www.cdc.gov/nchs/data/nvsr/nvsr60/nvsr60_04.pdf . Accessed 19 Nov 2018.

4. Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, et al. Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation. 2007;115:361–7.

5. Filiano JJ, Kinney HC. A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model. Biol Neonate. 1994;65:194–7.

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