000 01427 a2200397 4500
005 20250515055315.0
264 0 _c20070712
008 200707s 0 0 eng d
022 _a0885-3185
024 7 _a10.1002/mds.21391
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFrédéric, Mélissa
245 0 0 _aFirst determination of the incidence of the unique TOR1A gene mutation, c.907delGAG, in a Mediterranean population.
_h[electronic resource]
260 _bMovement disorders : official journal of the Movement Disorder Society
_cApr 2007
300 _a884-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aDNA
_xblood
650 0 4 _aFrance
650 0 4 _aGene Amplification
650 0 4 _aHumans
650 0 4 _aIncidence
650 0 4 _aInfant, Newborn
650 0 4 _aMediterranean Islands
650 0 4 _aMolecular Chaperones
_xgenetics
650 0 4 _aMutation
650 0 4 _aSequence Deletion
700 1 _aLucarz, Estelle
700 1 _aMonino, Christine
700 1 _aSaquet, Céline
700 1 _aThorel, Delphine
700 1 _aClaustres, Mireille
700 1 _aTuffery-Giraud, Sylvie
700 1 _aCollod-Béroud, Gwenaelle
773 0 _tMovement disorders : official journal of the Movement Disorder Society
_gvol. 22
_gno. 6
_gp. 884-8
856 4 0 _uhttps://doi.org/10.1002/mds.21391
_zAvailable from publisher's website
999 _c16850524
_d16850524