000 01128 a2200349 4500
005 20250514022524.0
264 0 _c20020628
008 200206s 0 0 eng d
022 _a0141-8955
024 7 _a10.1023/a:1012905823879
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aJebnoun, S
245 0 0 _aA family study of congenital malabsorption of folate.
_h[electronic resource]
260 _bJournal of inherited metabolic disease
_cDec 2001
300 _a749-50 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aFemale
650 0 4 _aFolic Acid
_xblood
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntelligence Tests
650 0 4 _aLeucovorin
_xadministration & dosage
650 0 4 _aMalabsorption Syndromes
_xdrug therapy
650 0 4 _aMale
700 1 _aKacem, S
700 1 _aMokrani, C H
700 1 _aChabchoub, A
700 1 _aKhrouf, N
700 1 _aZittoun, J
773 0 _tJournal of inherited metabolic disease
_gvol. 24
_gno. 7
_gp. 749-50
856 4 0 _uhttps://doi.org/10.1023/a:1012905823879
_zAvailable from publisher's website
999 _c11714987
_d11714987