000 01865 a2200541 4500
005 20250513045026.0
264 0 _c19950228
008 199502s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/3.9.1647
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPetrukhin, K
245 0 0 _aCharacterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions.
_h[electronic resource]
260 _bHuman molecular genetics
_cSep 1994
300 _a1647-56 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdenosine Triphosphatases
_xchemistry
650 0 4 _aAlternative Splicing
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aBinding Sites
_xgenetics
650 0 4 _aBiological Evolution
650 0 4 _aBrain
_xenzymology
650 0 4 _aCation Transport Proteins
650 0 4 _aChromosome Mapping
650 0 4 _aCloning, Molecular
650 0 4 _aCopper
_xmetabolism
650 0 4 _aCopper-Transporting ATPases
650 0 4 _aDNA, Complementary
_xgenetics
650 0 4 _aFemale
650 0 4 _aHepatolenticular Degeneration
_xenzymology
650 0 4 _aHumans
650 0 4 _aIon Transport
650 0 4 _aKidney
_xenzymology
650 0 4 _aLiver
_xenzymology
650 0 4 _aMolecular Sequence Data
650 0 4 _aPlacenta
_xenzymology
650 0 4 _aPregnancy
650 0 4 _aStructure-Activity Relationship
650 0 4 _aTissue Distribution
700 1 _aLutsenko, S
700 1 _aChernov, I
700 1 _aRoss, B M
700 1 _aKaplan, J H
700 1 _aGilliam, T C
773 0 _tHuman molecular genetics
_gvol. 3
_gno. 9
_gp. 1647-56
856 4 0 _uhttps://doi.org/10.1093/hmg/3.9.1647
_zAvailable from publisher's website
999 _c7833262
_d7833262