000 01788 a2200541 4500
005 20250515131608.0
264 0 _c20081103
008 200811s 0 0 eng d
022 _a1096-7206
024 7 _a10.1016/j.ymgme.2008.06.007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCosson, M A
245 0 0 _aLiver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria.
_h[electronic resource]
260 _bMolecular genetics and metabolism
_c
300 _a107-9 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCells, Cultured
650 0 4 _aChild
650 0 4 _aElectron Transport
650 0 4 _aFatal Outcome
650 0 4 _aFibroblasts
_xenzymology
650 0 4 _aFollow-Up Studies
650 0 4 _aHepatoblastoma
_xenzymology
650 0 4 _aHumans
650 0 4 _aImmunosuppressive Agents
_xadverse effects
650 0 4 _aKidney
_xenzymology
650 0 4 _aKidney Transplantation
_xadverse effects
650 0 4 _aLipid Metabolism, Inborn Errors
_xcomplications
650 0 4 _aMale
650 0 4 _aMethylmalonic Acid
_xmetabolism
650 0 4 _aMethylmalonyl-CoA Mutase
_xgenetics
650 0 4 _aMutation
700 1 _aTouati, G
700 1 _aLacaille, F
700 1 _aValayannnopoulos, V
700 1 _aGuyot, C
700 1 _aGuest, G
700 1 _aVerkarre, V
700 1 _aChrétien, D
700 1 _aRabier, D
700 1 _aMunnich, A
700 1 _aBenoist, J F
700 1 _ade Keyzer, Y
700 1 _aNiaudet, P
700 1 _ade Lonlay, P
773 0 _tMolecular genetics and metabolism
_gvol. 95
_gno. 1-2
_gp. 107-9
856 4 0 _uhttps://doi.org/10.1016/j.ymgme.2008.06.007
_zAvailable from publisher's website
999 _c18151431
_d18151431