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