000 | 01260 a2200349 4500 | ||
---|---|---|---|
005 | 20250517113238.0 | ||
264 | 0 | _c20170726 | |
008 | 201707s 0 0 eng d | ||
022 | _a1476-5438 | ||
024 | 7 |
_a10.1038/ejhg.2016.113 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aRichardson, Tom G | |
245 | 0 | 0 |
_aA pathway-centric approach to rare variant association analysis. _h[electronic resource] |
260 |
_bEuropean journal of human genetics : EJHG _c01 2016 |
||
300 |
_a123-129 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aBiosynthetic Pathways _xgenetics |
650 | 0 | 4 | _aGenetic Association Studies |
650 | 0 | 4 | _aGenetic Diseases, Inborn |
650 | 0 | 4 | _aGenome, Human |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHigh-Throughput Nucleotide Sequencing |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMolecular Sequence Annotation |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
700 | 1 | _aTimpson, Nicholas J | |
700 | 1 | _aCampbell, Colin | |
700 | 1 | _aGaunt, Tom R | |
773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 25 _gno. 1 _gp. 123-129 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1038/ejhg.2016.113 _zAvailable from publisher's website |
999 |
_c26374866 _d26374866 |