Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency

Blood

Volumn 103, Issue 4, 2004, Pages 1515-1517

  Yassin, Fawwaz ^b   Rothenberg, Sheldon P ^b   Rao, Sreedhar ^b   Gordon, Marilyn M ^b   Alpers, David H ^b   Quadros, Edward V ^a  

^a SUNY Downstate Medical Center   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANTISERUM; COBALAMIN; ENDONUCLEASE; INTRINSIC FACTOR; PENTAGASTRIN; PROTEIN BSTXI; UNCLASSIFIED DRUG;

ANEMIA; ARTICLE; BASE EXCISION; BONE MARROW EXAMINATION; CASE REPORT; CELL STRUCTURE; COBALAMIN MALADSORPTION; DISEASE SEVERITY; EXON; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENETIC CODE; HORMONE DEFICIENCY; HUMAN; IMMUNOPRECIPITATION; INHERITANCE; INTRINSIC FACTOR DEFICIENCY; INTRON; MALABSORPTION; MEGALOBLASTIC ANEMIA; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN BINDING; SCHILLING TEST; SCHOOL CHILD; STOMACH ACID SECRETION; STOMACH JUICE; TRANSLATION REGULATION;

EID: 0842307311     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2003-07-2239     Document Type: Article

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