000 01820 a2200565 4500
005 20250515005039.0
264 0 _c20060203
008 200602s 0 0 eng d
022 _a1061-4036
024 7 _a10.1038/ng1680
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMonsuur, Alienke J
245 0 0 _aMyosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.
_h[electronic resource]
260 _bNature genetics
_cDec 2005
300 _a1341-4 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAmino Acid Sequence
650 0 4 _aCeliac Disease
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aIntestine, Small
_xphysiopathology
650 0 4 _aIntrons
_xgenetics
650 0 4 _aMale
650 0 4 _aMolecular Sequence Data
650 0 4 _aMyosins
_xgenetics
650 0 4 _aPolymorphism, Single Nucleotide
700 1 _ade Bakker, Paul I W
700 1 _aAlizadeh, Behrooz Z
700 1 _aZhernakova, Alexandra
700 1 _aBevova, Marianna R
700 1 _aStrengman, Eric
700 1 _aFranke, Lude
700 1 _avan't Slot, Ruben
700 1 _avan Belzen, Martine J
700 1 _aLavrijsen, Ineke C M
700 1 _aDiosdado, BegoƱa
700 1 _aDaly, Mark J
700 1 _aMulder, Chris J J
700 1 _aMearin, M Luisa
700 1 _aMeijer, Jos W R
700 1 _aMeijer, Gerrit A
700 1 _avan Oort, Erica
700 1 _aWapenaar, Martin C
700 1 _aKoeleman, Bobby P C
700 1 _aWijmenga, Cisca
773 0 _tNature genetics
_gvol. 37
_gno. 12
_gp. 1341-4
856 4 0 _uhttps://doi.org/10.1038/ng1680
_zAvailable from publisher's website
999 _c15907529
_d15907529