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