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[Megaloblastic anemia in selective disorder of vitamin B12 resorption with proteinuria and antibody deficiency syndrome--a genetic defect].

AuthorsH Goebell, K Havemann, V Herbert
JournalVerhandlungen der Deutschen Gesellschaft fur Innere Medizin (Verh Dtsch Ges Inn Med) Vol. 78 Pg. 179-80 ( 1972) ISSN: 0070-4067 [Print] Germany
Vernacular TitleMegaloblastäre Anämie bei selektiver Störung der Vitamin B 12-Resorption mit Proteinurie und Antikörpermangelsyndrom--ein genetischer Defekt.
PMID4665640 (Publication Type: Journal Article)
Chemical References
  • Intrinsic Factor
  • Vitamin B 12
Topics
  • Adolescent
  • Anemia, Macrocytic (complications)
  • Humans
  • Immunologic Deficiency Syndromes (complications)
  • Intrinsic Factor (metabolism)
  • Malabsorption Syndromes (complications)
  • Male
  • Proteinuria (complications)
  • Vitamin B 12 (metabolism)
  • Vitamin B 12 Deficiency (etiology)

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