000 01346 a2200385 4500
005 20250511193554.0
264 0 _c19920702
008 199207s 0 0 eng d
022 _a0022-3476
024 7 _a10.1016/s0022-3476(05)81967-5
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGeraghty, M T
245 0 0 _aCobalamin C defect associated with hemolytic-uremic syndrome.
_h[electronic resource]
260 _bThe Journal of pediatrics
_cJun 1992
300 _a934-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aFemale
650 0 4 _aGenes, Recessive
650 0 4 _aHemolytic-Uremic Syndrome
_xcomplications
650 0 4 _aHomocystinuria
_xcomplications
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMetabolism, Inborn Errors
_xcomplications
650 0 4 _aMethylmalonic Acid
_xurine
650 0 4 _aPhenotype
650 0 4 _aVitamin B 12
_xmetabolism
700 1 _aPerlman, E J
700 1 _aMartin, L S
700 1 _aHayflick, S J
700 1 _aCasella, J F
700 1 _aRosenblatt, D S
700 1 _aValle, D
773 0 _tThe Journal of pediatrics
_gvol. 120
_gno. 6
_gp. 934-7
856 4 0 _uhttps://doi.org/10.1016/s0022-3476(05)81967-5
_zAvailable from publisher's website
999 _c1599837
_d1599837