| 000 | 01515 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250514225755.0 | ||
| 264 | 0 | _c20050829 | |
| 008 | 200508s 0 0 eng d | ||
| 022 | _a0002-9297 | ||
| 024 | 7 |
_a10.1086/431426 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZareparsi, Sepideh | |
| 245 | 0 | 0 |
_aStrong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration. _h[electronic resource] |
| 260 |
_bAmerican journal of human genetics _cJul 2005 |
||
| 300 |
_a149-53 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 1 |
| 650 | 0 | 4 |
_aComplement Factor H _xgenetics |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMacular Degeneration _xgenetics |
| 650 | 0 | 4 | _aModels, Genetic |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aRisk |
| 700 | 1 | _aBranham, Kari E H | |
| 700 | 1 | _aLi, Mingyao | |
| 700 | 1 | _aShah, Sapna | |
| 700 | 1 | _aKlein, Robert J | |
| 700 | 1 | _aOtt, Jurg | |
| 700 | 1 | _aHoh, Josephine | |
| 700 | 1 | _aAbecasis, Gonçalo R | |
| 700 | 1 | _aSwaroop, Anand | |
| 773 | 0 |
_tAmerican journal of human genetics _gvol. 77 _gno. 1 _gp. 149-53 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1086/431426 _zAvailable from publisher's website |
| 999 |
_c15557778 _d15557778 |
||