Exome Sequencing, ANGPTL3 Mutations, and Familial Combined Hypolipidemia
- Author
- MUSUNURU, Kiran1 2 4 7 8 ; PIRRUCCELLO, James P1 2 7 8 ; FENNELL, Tim7 ; BANKS, Eric7 ; AMBROGIO, Lauren7 ; CIBULSKIS, Kristian7 ; KERNYTSKY, Andrew7 ; GONZALEZ, Elena7 ; RUDZICZ, Nicholas9 ; ENGERT, James C9 ; DEPRISTO, Mark A7 ; DALY, Mark J2 4 7 ; DO, Ron1 2 7 9 ; COHEN, Jonathan C11 ; HOBBS, Helen H11 ; ALTSHULER, David2 3 4 5 7 ; SCHONFELD, Gustav12 ; GABRIEL, Stacey B7 ; PIN YUE12 ; KATHIRESAN, Sekar2 4 7 ; PELOSO, Gina M10 6 ; GUIDUCCI, Candace7 ; SOUGNEZ, Carrie7 ; GARIMELLA, Kiran V7 ; FISHER, Sheila7 ; ABREU, Justin7 ; BARRY, Andrew J7
[1] Cardiovascular Research Center, Massachusetts General Hospital, United States
[2] Center for Human Genetic Research, Massachusetts General Hospital, United States
[3] Department of Molecular Biology, Massachusetts General Hospital, United States
[4] Department of Medicine, Harvard Medical School, United States
[5] Department of Genetics, Harvard Medical School, United States
[6] Department of Biostatistics, Boston University School of Public Health, Boston, United States
[7] Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, United States
[8] Johns Hopkins University School of Medicine, Baltimore, United States
[9] Department of Human Genetics, McGill University, Montreal, Canada
[10] Framingham Heart Study of the National Heart, Lung, and Blood Institute, Framingham, MA, United States
[11] Departments of Molecular Genetics and Internal Medicine, University of Texas Southwestern Medical Center at Dallas, Dallas, United States
[12] Washington University in St. Louis School of Medicine, St. Louis, United States - Source
The New England journal of medicine. 2010, Vol 363, Num 23, pp 2220-2227, 8 p ; ref : 22 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Waltham, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Etude familiale Génétique Mutation Médecine Séquence nucléotide Séquençage
- Keyword (en)
- Family study Genetics Mutation Medicine Nucleotide sequence Sequencing
- Keyword (es)
- Estudio familiar Genética Mutación Medicina Secuencia nucleótido Sequencing
- Classification
- Discipline
- Generalities in medical sciences
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 23619972
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1056/NEJMoa1002926 
https://dx.doi.org/10.1056/NEJMoa1002926
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