000 01472 a2200409 4500
005 20250514234459.0
264 0 _c20051027
008 200510s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/ddi292
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSriram, Sathya R
245 0 0 _aFamilial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkin.
_h[electronic resource]
260 _bHuman molecular genetics
_cSep 2005
300 _a2571-86 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aHeterozygote
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aMutation, Missense
650 0 4 _aParkinson Disease
_xgenetics
650 0 4 _aPoint Mutation
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aProtein Binding
650 0 4 _aSolubility
650 0 4 _aUbiquitin
_xmetabolism
650 0 4 _aUbiquitin-Protein Ligases
_xchemistry
700 1 _aLi, Xiaojie
700 1 _aKo, Han Seok
700 1 _aChung, Kenny K K
700 1 _aWong, Esther
700 1 _aLim, Kah Leong
700 1 _aDawson, Valina L
700 1 _aDawson, Ted M
773 0 _tHuman molecular genetics
_gvol. 14
_gno. 17
_gp. 2571-86
856 4 0 _uhttps://doi.org/10.1093/hmg/ddi292
_zAvailable from publisher's website
999 _c15702522
_d15702522