000 | 01981 a2200625 4500 | ||
---|---|---|---|
005 | 20250516061813.0 | ||
264 | 0 | _c20120120 | |
008 | 201201s 0 0 eng d | ||
022 | _a1546-1718 | ||
024 | 7 |
_a10.1038/ng.976 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aRaychaudhuri, Soumya | |
245 | 0 | 0 |
_aA rare penetrant mutation in CFH confers high risk of age-related macular degeneration. _h[electronic resource] |
260 |
_bNature genetics _cOct 2011 |
||
300 |
_a1232-6 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAged |
650 | 0 | 4 | _aAged, 80 and over |
650 | 0 | 4 | _aCase-Control Studies |
650 | 0 | 4 |
_aComplement Factor H _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenetic Predisposition to Disease |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHigh-Throughput Nucleotide Sequencing |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aLinkage Disequilibrium |
650 | 0 | 4 |
_aMacular Degeneration _xgenetics |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aPenetrance |
650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
650 | 0 | 4 | _aPrincipal Component Analysis |
650 | 0 | 4 | _aRisk Factors |
650 | 0 | 4 | _aSequence Analysis, DNA |
700 | 1 | _aIartchouk, Oleg | |
700 | 1 | _aChin, Kimberly | |
700 | 1 | _aTan, Perciliz L | |
700 | 1 | _aTai, Albert K | |
700 | 1 | _aRipke, Stephan | |
700 | 1 | _aGowrisankar, Sivakumar | |
700 | 1 | _aVemuri, Soumya | |
700 | 1 | _aMontgomery, Kate | |
700 | 1 | _aYu, Yi | |
700 | 1 | _aReynolds, Robyn | |
700 | 1 | _aZack, Donald J | |
700 | 1 | _aCampochiaro, Betsy | |
700 | 1 | _aCampochiaro, Peter | |
700 | 1 | _aKatsanis, Nicholas | |
700 | 1 | _aDaly, Mark J | |
700 | 1 | _aSeddon, Johanna M | |
773 | 0 |
_tNature genetics _gvol. 43 _gno. 12 _gp. 1232-6 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1038/ng.976 _zAvailable from publisher's website |
999 |
_c21251455 _d21251455 |