The molecular basis of Sjogren-Larsson syndrome: Mutation analysis of the fatty aldehyde dehydrogenase gene

American Journal of Human Genetics

Volumn 65, Issue 6, 1999, Pages 1547-1560

  Rizzo, William B ^a   Carney, Gael ^a   Lin, Zhili ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DEHYDROGENASE; LONG CHAIN ALDEHYDE DEHYDROGENASE; LONG-CHAIN-ALDEHYDE DEHYDROGENASE; MESSENGER RNA;

AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; GENE DELETION; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC RECOMBINATION; GENETIC STABILITY; HUMAN; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RNA SPLICING; SJOEGREN LARSSON SYNDROME; ALLELE; ALTERNATIVE RNA SPLICING; CATALYSIS; CELL LINE; ENZYMOLOGY; EXON; FAMILY HEALTH; GENE FREQUENCY; GENETIC VARIABILITY; GENETICS; HAPLOTYPE; INTRON; METABOLISM; MUTATION; RECESSIVE GENE; RNA STABILITY; STOP CODON;

MAMMALIA;

ALDEHYDE OXIDOREDUCTASES; ALLELES; ALTERNATIVE SPLICING; BASE SEQUENCE; CATALYSIS; CELL LINE; CODON, TERMINATOR; EXONS; FAMILY HEALTH; GENE FREQUENCY; GENES, RECESSIVE; HAPLOTYPES; HUMANS; INTRONS; MUTATION; POLYMORPHISM, GENETIC; RNA STABILITY; RNA, MESSENGER; SJOGREN-LARSSON SYNDROME; VARIATION (GENETICS);

EID: 0033233482     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302681     Document Type: Article

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