000 01528 a2200493 4500
005 20250513192332.0
264 0 _c19991101
008 199911s 0 0 eng d
022 _a1018-4813
024 7 _a10.1038/sj.ejhg.5200343
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMüller, C R
245 0 0 _aAllelic heterogeneity of alkaptonuria in Central Europe.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_cSep 1999
300 _a645-51 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAlkaptonuria
_xethnology
650 0 4 _aAlleles
650 0 4 _aAlternative Splicing
650 0 4 _aDNA, Complementary
_xanalysis
650 0 4 _aEurope
_xepidemiology
650 0 4 _aExons
650 0 4 _aFounder Effect
650 0 4 _aGenetic Heterogeneity
650 0 4 _aGenetic Markers
650 0 4 _aGenetic Testing
650 0 4 _aHumans
650 0 4 _aIntrons
650 0 4 _aMutation
650 0 4 _aMutation, Missense
650 0 4 _aPoint Mutation
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aRecombinant Proteins
_xmetabolism
650 0 4 _aTime Factors
700 1 _aFregin, A
700 1 _aSrsen, S
700 1 _aSrsnova, K
700 1 _aHalliger-Keller, B
700 1 _aFelbor, U
700 1 _aSeemanova, E
700 1 _aKress, W
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 7
_gno. 6
_gp. 645-51
856 4 0 _uhttps://doi.org/10.1038/sj.ejhg.5200343
_zAvailable from publisher's website
999 _c10440344
_d10440344