Autozygome Sequencing Expands the Horizon of Human Knockout Research and Provides Novel Insights into Human Phenotypic Variation

PLoS Genetics

Volumn 9, Issue 12, 2013, Pages

  Alsalem, Ahmed B ^a,b   Halees, Anason S ^a   Anazi, Shamsa ^a   Alshamekh, Shomoukh ^c   Alkuraya, Fowzan S ^a,d  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^b KING SAUD BIN ABDULAZIZ UNIVERSITY FOR HEALTH SCIENCES   (Saudi Arabia)

^c KING ABDUL AZIZ UNIVERSITY HOSPITAL   (Saudi Arabia)

^d ALFAISAL UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOZYGOSITY; BIOINFORMATICS; CONTROLLED STUDY; EXOME; FERTILITY; FRAMESHIFT MUTATION; GENE ACTIVATION; GENE FREQUENCY; GENE IDENTIFICATION; GENE MAPPING; GENE SEQUENCE; GENETIC VARIABILITY; GENOME ANALYSIS; HOMOZYGOSITY; HUMAN; IMMUNITY; KNOCKOUT GENE; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; METABOLIC REGULATION; NONSENSE MUTATION; PERCEPTION; PHENOTYPIC VARIATION; PSEUDOGENE; SINGLE NUCLEOTIDE POLYMORPHISM; ZYGOSITY;

CONSANGUINITY; EXOME; GENE KNOCKOUT TECHNIQUES; GENE SILENCING; GENES, RECESSIVE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HOMOZYGOTE; HUMANS; MUTATION; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84892688767     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1004030     Document Type: Article

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