000 01684 a2200493 4500
005 20250513230354.0
264 0 _c20010607
008 200106s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/10.4.361
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLa Fontaine , S
245 0 0 _aEffect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase.
_h[electronic resource]
260 _bHuman molecular genetics
_cFeb 2001
300 _a361-70 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdenosine Triphosphatases
_xbiosynthesis
650 0 4 _aAnimals
650 0 4 _aCHO Cells
650 0 4 _aCarrier Proteins
_xbiosynthesis
650 0 4 _aCation Transport Proteins
650 0 4 _aCopper
_xmetabolism
650 0 4 _aCopper-Transporting ATPases
650 0 4 _aCricetinae
650 0 4 _aFemale
650 0 4 _aHepatolenticular Degeneration
_xgenetics
650 0 4 _aHumans
650 0 4 _aIntracellular Fluid
_xmetabolism
650 0 4 _aMenkes Kinky Hair Syndrome
_xgenetics
650 0 4 _aMice
650 0 4 _aMice, Inbred BALB C
650 0 4 _aMilk
_xtoxicity
650 0 4 _aMutation
650 0 4 _aRecombinant Fusion Proteins
650 0 4 _aSequence Homology, Amino Acid
650 0 4 _aTransfection
700 1 _aTheophilos, M B
700 1 _aFirth, S D
700 1 _aGould, R
700 1 _aParton, R G
700 1 _aMercer, J F
773 0 _tHuman molecular genetics
_gvol. 10
_gno. 4
_gp. 361-70
856 4 0 _uhttps://doi.org/10.1093/hmg/10.4.361
_zAvailable from publisher's website
999 _c11097389
_d11097389