000 01763 a2200541 4500
005 20250516005730.0
264 0 _c20110202
008 201102s 0 0 eng d
022 _a1432-1203
024 7 _a10.1007/s00439-010-0897-1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPiret, Sian E
245 0 0 _aGenome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.
_h[electronic resource]
260 _bHuman genetics
_cJan 2011
300 _a51-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChromosomes, Human, Pair 2
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Heterogeneity
650 0 4 _aGenetic Linkage
650 0 4 _aGenetic Loci
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenome, Human
650 0 4 _aGenome-Wide Association Study
650 0 4 _aGout
_xgenetics
650 0 4 _aHumans
650 0 4 _aHyperuricemia
_xgenetics
650 0 4 _aKidney Diseases
_xgenetics
650 0 4 _aKidney Failure, Chronic
_xgenetics
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aUric Acid
_xblood
700 1 _aDanoy, Patrick
700 1 _aDahan, Karin
700 1 _aReed, Anita A C
700 1 _aPryce, Karena
700 1 _aWong, William
700 1 _aTorres, Rosa J
700 1 _aPuig, Juan G
700 1 _aMüller, Thomas
700 1 _aKotanko, Peter
700 1 _aLhotta, Karl
700 1 _aDevuyst, Olivier
700 1 _aBrown, Matthew A
700 1 _aThakker, Rajesh V
773 0 _tHuman genetics
_gvol. 129
_gno. 1
_gp. 51-8
856 4 0 _uhttps://doi.org/10.1007/s00439-010-0897-1
_zAvailable from publisher's website
999 _c20277377
_d20277377