000 | 01793 a2200553 4500 | ||
---|---|---|---|
005 | 20250514011135.0 | ||
264 | 0 | _c20011204 | |
008 | 200112s 0 0 eng d | ||
022 | _a0954-691X | ||
024 | 7 |
_a10.1097/00042737-200109000-00014 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aVan Vlierberghe, H | |
245 | 0 | 0 |
_aAssociation between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C. _h[electronic resource] |
260 |
_bEuropean journal of gastroenterology & hepatology _cSep 2001 |
||
300 |
_a1077-81 p. _bdigital |
||
500 | _aPublication Type: Comparative Study; Journal Article | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAged |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 | _aCase-Control Studies |
650 | 0 | 4 | _aChi-Square Distribution |
650 | 0 | 4 | _aCohort Studies |
650 | 0 | 4 |
_aCysteine _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aGenetic Predisposition to Disease _xepidemiology |
650 | 0 | 4 | _aGenetic Testing |
650 | 0 | 4 |
_aHaptoglobins _xanalysis |
650 | 0 | 4 |
_aHepatitis C, Chronic _xepidemiology |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aPolymorphism, Genetic |
650 | 0 | 4 | _aPrevalence |
650 | 0 | 4 | _aProbability |
650 | 0 | 4 | _aReference Values |
650 | 0 | 4 | _aRisk Assessment |
650 | 0 | 4 |
_aTyrosine _xgenetics |
700 | 1 | _aDelanghe, J R | |
700 | 1 | _aDe Bie, S | |
700 | 1 | _aPraet, M | |
700 | 1 | _aDe Paepe, A | |
700 | 1 | _aMessiaen, L | |
700 | 1 | _aDe Vos, M | |
700 | 1 | _aLeroux-Roels, G | |
773 | 0 |
_tEuropean journal of gastroenterology & hepatology _gvol. 13 _gno. 9 _gp. 1077-81 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1097/00042737-200109000-00014 _zAvailable from publisher's website |
999 |
_c11486972 _d11486972 |