000 01300 a2200373 4500
005 20250518031928.0
264 0 _c20200415
008 202004s 0 0 eng d
022 _a1096-9896
024 7 _a10.1002/path.5271
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBashford, Andrew L
245 0 0 _aMice with a conditional deletion of Talpid3 (KIAA0586) - a model for Joubert syndrome.
_h[electronic resource]
260 _bThe Journal of pathology
_c08 2019
300 _a396-408 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAnimals
650 0 4 _aCell Cycle Proteins
_xdeficiency
650 0 4 _aCerebellum
_xabnormalities
650 0 4 _aDisease Models, Animal
650 0 4 _aExons
650 0 4 _aEye Abnormalities
_xgenetics
650 0 4 _aGenetic Markers
650 0 4 _aKidney Diseases, Cystic
_xgenetics
650 0 4 _aMice
650 0 4 _aMice, Knockout
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aRetina
_xabnormalities
650 0 4 _aSequence Deletion
700 1 _aSubramanian, Vasanta
773 0 _tThe Journal of pathology
_gvol. 248
_gno. 4
_gp. 396-408
856 4 0 _uhttps://doi.org/10.1002/path.5271
_zAvailable from publisher's website
999 _c29529081
_d29529081