Location of the mutation site in the first two reported cases of analbuminemia

Clinical Biochemistry

Volumn 43, Issue 4-5, 2010, Pages 525-527

  Ruhoff, Mary S ^a   Greene, Michael W ^a   Peters, Theodore ^a  

^a BASSETT MEDICAL CENTER   (United States)

Author keywords

Albumin; Analbuminemia; Human; Mutation

Indexed keywords

ALBUMIN; ARGININE; CYSTEINE; DNA; THREONINE;

AMINO ACID SUBSTITUTION; ANALBUMINEMIA; ARTICLE; CONTROLLED STUDY; DNA EXTRACTION; DNA SEQUENCE; EXON; GENE AMPLIFICATION; GENE LOCATION; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; HUMAN TISSUE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STOP CODON;

ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; BLOOD PROTEIN DISORDERS; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; SERUM ALBUMIN; YOUNG ADULT;

EID: 76749088898     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2009.12.002     Document Type: Article

References (7)

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