Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: Evolutionary evidence for differences in molecular effects

Proceedings of the National Academy of Sciences of the United States of America

Volumn 101, Issue 43, 2004, Pages 15398-15403

  Thomas, Paul D ^a   Kejariwal, Anish ^a  

^a APPLIED BIOSYSTEMS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; PROTEIN;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC DISORDER; GENETIC VARIABILITY; HUMAN; MENDELIAN DISEASE; MOLECULAR BIOLOGY; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; PROBABILITY; PROTEIN FUNCTION; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; STANDARDIZATION; STATISTICAL ANALYSIS;

EVOLUTION; GENETIC DISEASES, INBORN; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 7444227970     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0404380101     Document Type: Article

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