Identification of a large set of rare complete human knockouts

Nature Genetics

Volumn 47, Issue 5, 2015, Pages 448-452

  Sulem, Patrick ^a   Helgason, Hannes ^a,b   Oddson, Asmundur ^a   Stefansson, Hreinn ^a   Gudjonsson, Sigurjon A ^a   Zink, Florian ^a   Hjartarson, Eirikur ^a   Sigurdsson, Gunnar Th ^a   Jonasdottir, Adalbjorg ^a   Jonasdottir, Aslaug ^a   Sigurdsson, Asgeir ^a   Magnusson, Olafur Th ^a   Kong, Augustine ^a,b   Helgason, Agnar ^a,b   Holm, Hilma ^a,c   Thorsteinsdottir, Unnur ^a,d   Masson, Gisli ^a   Gudbjartsson, Daniel F ^a,b   Stefansson, Kari ^a,d  

^a DECODE GENETICS   (Iceland)

^b UNIVERSITY OF ICELAND   (Iceland)

^c LANDSPITALI UNIVERSITY HOSPITAL   (Iceland)

^d UNIVERSITY OF ICELAND   (Iceland)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL TISSUE; ARTICLE; AUTOSOMAL GENE; BRAIN; CONTROLLED STUDY; GENE; GENE FREQUENCY; GENE SEQUENCE; GENOME; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HUMAN TISSUE; ICELANDER; INDEL MUTATION; LOSS OF FUNCTION MUTATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROGENY; SINGLE NUCLEOTIDE POLYMORPHISM; ANTIBODY SPECIFICITY; DNA SEQUENCE; FEMALE; GENE EXPRESSION; GENE ONTOLOGY; HUMAN GENOME; MALE; METABOLISM; OPEN READING FRAME;

BRAIN; FEMALE; GENE EXPRESSION; GENE FREQUENCY; GENE ONTOLOGY; GENOME, HUMAN; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INDEL MUTATION; MALE; OPEN READING FRAMES; ORGAN SPECIFICITY; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA;

EID: 84929133372     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.3243     Document Type: Article

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