000 01307 a2200397 4500
005 20250512093054.0
264 0 _c19690807
008 196908s 0 0 eng d
022 _a0140-6736
024 7 _a10.1016/s0140-6736(69)92597-5
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOsborn, S B
245 0 0 _aThe influence of genetic and acquired liver defects on radio-copper turnover in Wilson's disease.
_h[electronic resource]
260 _bLancet (London, England)
_cJul 1969
300 _a17-20 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdult
650 0 4 _aBiopsy
650 0 4 _aChild
650 0 4 _aChronic Disease
650 0 4 _aCopper
_xblood
650 0 4 _aHepatitis
_xmetabolism
650 0 4 _aHepatolenticular Degeneration
_xcomplications
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aLiver
_xmetabolism
650 0 4 _aLiver Cirrhosis
_xmetabolism
650 0 4 _aLiver Function Tests
650 0 4 _aMiddle Aged
650 0 4 _aNeurologic Manifestations
650 0 4 _aRadioisotopes
650 0 4 _aSplenomegaly
_xcomplications
700 1 _aWalshe, J M
773 0 _tLancet (London, England)
_gvol. 2
_gno. 7610
_gp. 17-20
856 4 0 _uhttps://doi.org/10.1016/s0140-6736(69)92597-5
_zAvailable from publisher's website
999 _c4188186
_d4188186