000 01211 a2200361 4500
005 20250515063924.0
264 0 _c20070713
008 200707s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.31671
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBen-Omran, Tawfeg I
245 0 0 _aLate-onset cobalamin-C disorder: a challenging diagnosis.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cMay 2007
300 _a979-84 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAge of Onset
650 0 4 _aBrain Diseases, Metabolic, Inborn
_xdiagnosis
650 0 4 _aCarrier Proteins
_xgenetics
650 0 4 _aDementia
_xdiagnosis
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aOxidoreductases
650 0 4 _aPoint Mutation
650 0 4 _aVitamin B 12
_xmetabolism
700 1 _aWong, Hubert
700 1 _aBlaser, Susan
700 1 _aFeigenbaum, Annette
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 143A
_gno. 9
_gp. 979-84
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.31671
_zAvailable from publisher's website
999 _c16982544
_d16982544