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Volumn 150, Issue 3, 2010, Pages 369-371

Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIF

Author keywords

haemolysis; hereditary cobalamin deficiency; intrinsic factor deficiency; pancytopenia; vitamin B12

Indexed keywords

COBALAMIN; HEMOGLOBIN; INTRINSIC FACTOR;

EID: 77954596475     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2010.08198.x     Document Type: Letter
Times cited : (6)

References (9)
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  • 3
    • 1442357042 scopus 로고    scopus 로고
    • The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless
    • Fyfe, J.C., Madsen, M., Højrup, P., Christensen, E.I., Tanner, S.M., de la Chapelle, A., He, Q. Moestrup, S.K. (2004) The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood, 103, 1573 1579.
    • (2004) Blood , vol.103 , pp. 1573-1579
    • Fyfe, J.C.1    Madsen, M.2    Højrup, P.3    Christensen, E.I.4    Tanner, S.M.5    De La Chapelle, A.6    He, Q.7    Moestrup, S.K.8
  • 4
    • 34248165629 scopus 로고    scopus 로고
    • Imerslund-Gräsbeck syndrome (selective vitamin B(12) absorption with proteinuria
    • Gräsbeck, R. (2006) Imerslund-Gräsbeck syndrome (selective vitamin B(12) absorption with proteinuria. Orphanet Journal of Rare Diseases, 1, 17.
    • (2006) Orphanet Journal of Rare Diseases , vol.1 , pp. 17
    • Gräsbeck, R.1
  • 5
    • 72649089540 scopus 로고    scopus 로고
    • Advances in the understanding of cobalamin assimilation and metabolism
    • Quadros, E.V. (2009) Advances in the understanding of cobalamin assimilation and metabolism. British Journal of Haematology, 148, 195 204.
    • (2009) British Journal of Haematology , vol.148 , pp. 195-204
    • Quadros, E.V.1
  • 8
    • 0842307311 scopus 로고    scopus 로고
    • Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency
    • Yassin, F., Rothenberg, S.P., Rao, S., Gordon, M.M., Alpers, D.H. Quadros, E.V. (2004) Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency. Blood, 103, 1515 1517.
    • (2004) Blood , vol.103 , pp. 1515-1517
    • Yassin, F.1    Rothenberg, S.P.2    Rao, S.3    Gordon, M.M.4    Alpers, D.H.5    Quadros, E.V.6
  • 9
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    • Familial selective vitamin B12 malabsorption in three families
    • Yetgin, S., Altay, C. Laleli, Y. (1978) Familial selective vitamin B12 malabsorption in three families. Turkish Journal of Pediatrics, 20, 44 50.
    • (1978) Turkish Journal of Pediatrics , vol.20 , pp. 44-50
    • Yetgin, S.1    Altay, C.2    Laleli, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.