Juvenile selective vitamin B12 malabsorption: 50 years after its description-10 years of genetic testing

Pediatric Research

Volumn 70, Issue 3, 2011, Pages 222-228

  Gräsbeck, Ralph ^a   Tanner, Stephan M ^b  

^a MINERVA FOUNDATION INSTITUTE FOR MEDICAL RESEARCH   (Finland)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; HYDROXOCOBALAMIN; INTRINSIC FACTOR;

ABSENCE OF SIDE EFFECTS; AMBLYOPIA; AUTOSOMAL RECESSIVE DISORDER; AWARENESS; CHROMOSOME 10; CONGENITAL DISORDER; COST EFFECTIVENESS ANALYSIS; CYANOCOBALAMIN DEFICIENCY; CYANOCOBALAMIN MALABSORPTION; DRUG SUBSTITUTION; ETHNICITY; EUROPE; GENE MUTATION; GENETIC SCREENING; GENETICS; HUMAN; IMERSLUND GRASBECK SYNDROME; IMMIGRANT; INSTRINSIC FACTOR DEFICIENCY; KIDNEY ANOMALY; KIDNEY BIOPSY; LABORATORY TEST; MALABSORPTION; MIDDLE EAST; MUTATIONAL ANALYSIS; MYALGIA; NORTH AFRICA; NORTH AMERICA; PERNICIOUS ANEMIA; PRIORITY JOURNAL; PROTEINURIA; REVIEW;

DNA MUTATIONAL ANALYSIS; GENETIC TESTING; HUMANS; MALABSORPTION SYNDROMES; SCHILLING TEST; VITAMIN B 12; VITAMIN B 12 DEFICIENCY;

EID: 80051715810     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3182242124     Document Type: Review

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