Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia

Journal of Human Genetics

Volumn 47, Issue 7, 2002, Pages 355-359

  Asada Senju, Midori ^a,b   Maeda, Toyoki ^a   Sakata, Toshiie ^b   Hayashi, Akira ^c   Suzuki, TomoKazu ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b OITA UNIVERSITY   (Japan)

^c OSAKA MEDICAL CENTER FOR CANCER AND CARDIOVASCULAR DISEASES   (Japan)

Author keywords

Familial hypotransferrinemia; Gene analysis; Mutation; PCR RFLP; Transferrin

Indexed keywords

MESSENGER RNA; MUTANT PROTEIN; TRANSFERRIN;

ALLELE; AMINO ACID SUBSTITUTION; ANEMIA; ARTICLE; BINDING SITE; CASE REPORT; CONFORMATIONAL TRANSITION; EXON; FAMILY STUDY; GROWTH RETARDATION; HEREDITARY HYPOTRANSFERRINEMIA; HETEROZYGOTE; HUMAN; INTRON; ISOELECTRIC FOCUSING; ISOELECTRIC POINT; MALE; NUCLEIC ACID BASE SUBSTITUTION; NULL ALLELE; PROTEIN DEFICIENCY; PROTEIN VARIANT; RNA STABILITY; RNA TRANSCRIPTION; TRANSFERRIN BLOOD LEVEL; GENETICS; METABOLISM; MISSENSE MUTATION;

AMINO ACID SUBSTITUTION; HUMANS; ISOELECTRIC FOCUSING; MUTATION, MISSENSE; TRANSFERRIN;

EID: 0036308217     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380200049     Document Type: Article

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