Understanding human disease mutations through the use of interspecific genetic variation

Human Molecular Genetics

Volumn 10, Issue 21, 2001, Pages 2319-2328

  Miller, Mark P ^a   Kumar, Sudhir ^a,b  

^a ARIZONA STATE UNIVERSITY   (United States)

^b UTAH STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; GENE PRODUCT; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; HOMEODOMAIN PROTEIN; NERVE CELL ADHESION MOLECULE; NERVE CELL ADHESION MOLECULE L1; PHENYLALANINE 4 MONOOXYGENASE; RS1 PROTEIN; TRANSCRIPTION FACTOR PAX6; TRANSMEMBRANE CONDUCTANCE REGULATOR; TUBERIN; UNCLASSIFIED DRUG;

ARTICLE; BIOMEDICINE; CHEMISTRY; COMPREHENSION; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CONSERVATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HISTORY; HUMAN; INFORMATION; METAZOON; MOLECULAR EVOLUTION; NONHUMAN; NUCLEOTIDE SEQUENCE; ONLINE SYSTEM; PRIORITY JOURNAL; RETINOSCHISIS; SEQUENCE HOMOLOGY; SPECIES DIFFERENCE; X CHROMOSOME LINKED DISORDER;

METAZOA;

EID: 0035504763     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.21.2319     Document Type: Article

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