000 01355 a2200361 4500
005 20250516013835.0
264 0 _c20110314
008 201103s 0 0 eng d
022 _a1470-8752
024 7 _a10.1042/BST0381453
_2doi
040 _aNLM
_beng
_cNLM
100 1 _ad'Azzo, Alessandra
245 0 0 _aMolecular mechanisms of pathogenesis in a glycosphingolipid and a glycoprotein storage disease.
_h[electronic resource]
260 _bBiochemical Society transactions
_cDec 2010
300 _a1453-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aCathepsin A
_xchemistry
650 0 4 _aDisease Models, Animal
650 0 4 _aGlycoproteins
_xmetabolism
650 0 4 _aGlycosphingolipids
_xmetabolism
650 0 4 _aHumans
650 0 4 _aLysosomal Storage Diseases
_xgenetics
650 0 4 _aLysosomes
_xmetabolism
650 0 4 _aModels, Molecular
650 0 4 _aMultienzyme Complexes
_xmetabolism
650 0 4 _aNeuraminidase
_xchemistry
650 0 4 _aProtein Conformation
650 0 4 _abeta-Galactosidase
_xchemistry
700 1 _aBonten, Erik
773 0 _tBiochemical Society transactions
_gvol. 38
_gno. 6
_gp. 1453-7
856 4 0 _uhttps://doi.org/10.1042/BST0381453
_zAvailable from publisher's website
999 _c20410346
_d20410346