000 01599 a2200469 4500
005 20250516224742.0
264 0 _c20150330
008 201503s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/s13023-014-0124-6
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHébert, Betty
245 0 0 _aRescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_cAug 2014
300 _a124 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aFragile X Mental Retardation Protein
_xgenetics
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aHumans
650 0 4 _aLarge-Conductance Calcium-Activated Potassium Channel alpha Subunits
_xphysiology
650 0 4 _aMice
650 0 4 _aMice, Knockout
650 0 4 _aPhenotype
700 1 _aPietropaolo, Susanna
700 1 _aMême, Sandra
700 1 _aLaudier, Béatrice
700 1 _aLaugeray, Anthony
700 1 _aDoisne, Nicolas
700 1 _aQuartier, Angélique
700 1 _aLefeuvre, Sandrine
700 1 _aGot, Laurence
700 1 _aCahard, Dominique
700 1 _aLaumonnier, Frédéric
700 1 _aCrusio, Wim E
700 1 _aPichon, Jacques
700 1 _aMenuet, Arnaud
700 1 _aPerche, Olivier
700 1 _aBriault, Sylvain
773 0 _tOrphanet journal of rare diseases
_gvol. 9
_gp. 124
856 4 0 _uhttps://doi.org/10.1186/s13023-014-0124-6
_zAvailable from publisher's website
999 _c24058065
_d24058065