A family study of congenital malabsorption of folate

Journal of Inherited Metabolic Disease

Volumn 24, Issue 7, 2001, Pages 749-750

  Jebnoun, S ^a   Kacem, S ^a   Mokrani, Ch ^a   Chabchoub, A ^a   Khrouf, N ^a   Zittoun, J ^b  

^a Centre de Maternite et de Neonatologie Tunis   (Tunisia)

^b CENTRE HOSPITALIER INTERCOMMUNAL DE CRÉTEIL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

5 METHYLTETRAHYDROFOLIC ACID; CYANOCOBALAMIN; DNA; FOLIC ACID; FOLINIC ACID; THYMIDINE;

ANEMIA; ARTICLE; BLOOD CELL COUNT; BLOOD SMEAR; BONE MARROW EXAMINATION; CASE REPORT; DOMINANT INHERITANCE; DOSE RESPONSE; FAMILY; FEMALE; FOLIC ACID BLOOD LEVEL; HUMAN; INFANT; JEJUNUM BIOPSY; LEUKOPENIA; LOADING TEST; MALABSORPTION; MALE; PANCYTOPENIA; SCHOOL CHILD; SYMPTOMATOLOGY; THROMBOCYTOPENIA;

FEMALE; FOLIC ACID; HUMANS; INFANT; INTELLIGENCE TESTS; LEUCOVORIN; MALABSORPTION SYNDROMES; MALE;

EID: 0035663592     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1012905823879     Document Type: Article

References (2)

1. Therapy of congenital folate malabsorption
2. 12 and folate deficiency