Literature DB >> 4756428

Inheritance of selective malabsorption of vitamin B12.

U Furuhjelm, H R Nevanlinna.   

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Year:  1973        PMID： 4756428     DOI： 10.1111/j.1600-0609.1973.tb00093.x

Source DB:  PubMed          Journal:  Scand J Haematol        ISSN： 0036-553X


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  4 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.

Authors:  M Aminoff; E Tahvanainen; R Gräsbeck; J Weissenbach; H Broch; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

3.  Absent ileal uptake of IF-bound vitamin B12 in vivo in the Imerslund-Grasbeck syndrome (familial vitamin B12 malabsorption with proteinuria).

Authors:  J F Burman; W J Jenkins; J A Walker-Smith; A D Phillips; N A Sourial; C B Williams; D L Mollin
Journal:  Gut       Date:  1985-03       Impact factor: 23.059

4.  Selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome). Studies on gastroenterological and nephrological problems.

Authors:  M Becker; H W Rotthauwe; H P Weber; H Fischbach
Journal:  Eur J Pediatr       Date:  1977-01-26       Impact factor: 3.183
  4 in total

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