000 01240 a2200325 4500
005 20250517005129.0
264 0 _c20151022
008 201510s 0 0 eng d
022 _a1531-8257
024 7 _a10.1002/mds.26096
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFogel, Brent L
245 0 0 _aDo mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
_h[electronic resource]
260 _bMovement disorders : official journal of the Movement Disorder Society
_cFeb 2015
300 _a284-6 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAtaxia
_xdiagnosis
650 0 4 _aBrain
_xpathology
650 0 4 _aGenetic Heterogeneity
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
_xgenetics
650 0 4 _aTRPC Cation Channels
_xgenetics
700 1 _aHanson, Sonya M
700 1 _aBecker, Esther B E
773 0 _tMovement disorders : official journal of the Movement Disorder Society
_gvol. 30
_gno. 2
_gp. 284-6
856 4 0 _uhttps://doi.org/10.1002/mds.26096
_zAvailable from publisher's website
999 _c24430353
_d24430353