000 01769 a2200529 4500
005 20250515161145.0
264 0 _c20090724
008 200907s 0 0 fre d
022 _a2213-0276
024 7 _a10.1016/j.lpm.2008.11.017
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTrocello, Jean-Marc
245 0 0 _a[Wilson disease].
_h[electronic resource]
260 _bPresse medicale (Paris, France : 1983)
_c
300 _a1089-98 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAdenosine Triphosphatases
_xgenetics
650 0 4 _aBrain
_xpathology
650 0 4 _aCation Transport Proteins
_xgenetics
650 0 4 _aChelating Agents
_xtherapeutic use
650 0 4 _aCopper
_xmetabolism
650 0 4 _aCopper Transport Proteins
650 0 4 _aCopper-Transporting ATPases
650 0 4 _aDisclosure
650 0 4 _aHepatocytes
_xmetabolism
650 0 4 _aHepatolenticular Degeneration
_xdrug therapy
650 0 4 _aHumans
650 0 4 _aIron
_xmetabolism
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMetallochaperones
650 0 4 _aMolecular Chaperones
_xgenetics
650 0 4 _aMonitoring, Physiologic
650 0 4 _aPatient Care Team
650 0 4 _aPenicillamine
_xtherapeutic use
650 0 4 _aPhenotype
650 0 4 _aRNA, Messenger
_xgenetics
650 0 4 _aRegistries
650 0 4 _aZinc
_xtherapeutic use
700 1 _aChappuis, Philippe
700 1 _aChaine, Pascal
700 1 _aRémy, Pascal
700 1 _aDebray, Dominique
700 1 _aDuclos-Vallée, Jean-Charles
700 1 _aWoimant, France
773 0 _tPresse medicale (Paris, France : 1983)
_gvol. 38
_gno. 7-8
_gp. 1089-98
856 4 0 _uhttps://doi.org/10.1016/j.lpm.2008.11.017
_zAvailable from publisher's website
999 _c18675995
_d18675995