| 000 | 01704 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250515232435.0 | ||
| 264 | 0 | _c20100907 | |
| 008 | 201009s 0 0 eng d | ||
| 022 | _a1432-1203 | ||
| 024 | 7 |
_a10.1007/s00439-010-0861-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTzur, Shay | |
| 245 | 0 | 0 |
_aMissense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene. _h[electronic resource] |
| 260 |
_bHuman genetics _cSep 2010 |
||
| 300 |
_a345-50 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAfrica |
| 650 | 0 | 4 | _aApolipoprotein L1 |
| 650 | 0 | 4 |
_aApolipoproteins _xgenetics |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aKidney Failure, Chronic _xgenetics |
| 650 | 0 | 4 | _aLinkage Disequilibrium |
| 650 | 0 | 4 |
_aLipoproteins, HDL _xgenetics |
| 650 | 0 | 4 |
_aMolecular Motor Proteins _xgenetics |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aMyosin Heavy Chains _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aRisk Factors |
| 700 | 1 | _aRosset, Saharon | |
| 700 | 1 | _aShemer, Revital | |
| 700 | 1 | _aYudkovsky, Guennady | |
| 700 | 1 | _aSelig, Sara | |
| 700 | 1 | _aTarekegn, Ayele | |
| 700 | 1 | _aBekele, Endashaw | |
| 700 | 1 | _aBradman, Neil | |
| 700 | 1 | _aWasser, Walter G | |
| 700 | 1 | _aBehar, Doron M | |
| 700 | 1 | _aSkorecki, Karl | |
| 773 | 0 |
_tHuman genetics _gvol. 128 _gno. 3 _gp. 345-50 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00439-010-0861-0 _zAvailable from publisher's website |
| 999 |
_c19977783 _d19977783 |
||