SCN1A variants associated with sudden infant death syndrome

Author:

Brownstein Catherine A.123,Goldstein Richard D.134,Thompson Christopher H.5,Haynes Robin L.16,Giles Emma16,Sheidley Beth7,Bainbridge Matthew8,Haas Elisabeth A.9,Mena Othon J.10,Lucas Jonathan10,Schaber Bethann10,Holm Ingrid A.123,George Alfred L.5,Kinney Hannah C.136,Poduri Annapurna H.171112

Affiliation:

1. Robert's Program on Sudden Death in Pediatrics; Boston Children's Hospital; Boston MA USA

2. Division of Genetics and Genomics; Manton Center for Orphan Disease Research; Boston Children's Hospital; Boston MA USA

3. Department of Pediatrics; Harvard Medical School; Boston MA USA

4. Department of Medicine; Division of General Pediatrics; Boston Children's Hospital; Boston MA USA

5. Department of Pharmacology; Feinberg School of Medicine; Northwestern University; Chicago IL USA

6. Department of Pathology; Boston Children's Hospital and Harvard Medical School; Boston MA USA

7. Epilepsy Genetics Program; Department of Neurology; Boston Children's Hospital; Boston MA USA

8. The Genomics Institute; Rady Children's Hospital; San Diego CA USA

9. Department of Pathology; Rady Children's Hospital-San Diego; San Diego CA USA

10. Office of the Medical Examiner; County of San Diego Medical Examiner's Office; San Diego CA USA

11. Department of Neurology; F. M. Kirby Neurobiology Center; Boston Children's Hospital; Boston MA USA

12. Department of Neurology; Harvard Medical School; Boston MA USA

Funder

National Institutes of Health

Boston Children's Hospital

Robert's Program on Sudden Unexpected Death in Pediatrics

Citizens United for Research in Epilepsy

Departments of Pathology, Pediatrics, and Neurology at Boston Children's Hospital

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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