Common polymorphic transcript variation in human disease

Genome Research

Volumn 19, Issue 4, 2009, Pages 567-575

  Fraser, Hunter B ^a,b   Xie, Xiaohui ^a,c  

^a BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^b ROSETTA INPHARMATICS   (United States)

^c Irvine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANKYLOSING SPONDYLITIS; ARTICLE; AUTOIMMUNE DISEASE; B LYMPHOCYTE; CONTROLLED STUDY; CROHN DISEASE; GENE EXPRESSION; GENE PROBE; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HUMAN; HUMAN CELL; INSULIN DEPENDENT DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RHEUMATOID ARTHRITIS; SINGLE NUCLEOTIDE POLYMORPHISM; UNTRANSLATED REGION;

B-LYMPHOCYTES; EXONS; GENETIC DISEASES, INBORN; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPES; HUMANS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN ISOFORMS; TRANSCRIPTION, GENETIC;

PERU TOMATO MOSAIC VIRUS;

EID: 63849281404     PISSN: 10889051     EISSN: 15495469     Source Type: Journal    
DOI: 10.1101/gr.083477.108     Document Type: Article

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