000 01457 a2200433 4500
005 20250516211053.0
264 0 _c20150226
008 201502s 0 0 eng d
022 _a1364-6753
024 7 _a10.1007/s10048-014-0404-2
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNicolas, Gaƫl
245 0 0 _aOverall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification.
_h[electronic resource]
260 _bNeurogenetics
_cAug 2014
300 _a215-6 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't; Comment
650 0 4 _aBasal Ganglia Diseases
_xgenetics
650 0 4 _aCalcinosis
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aNeurodegenerative Diseases
_xgenetics
650 0 4 _aSodium-Phosphate Cotransporter Proteins, Type III
_xgenetics
700 1 _aRichard, Anne-Claire
700 1 _aPottier, Cyril
700 1 _aVerny, Christophe
700 1 _aDurif, Franck
700 1 _aRoze, Emmanuel
700 1 _aFavrole, Pascal
700 1 _aRudolf, Gabrielle
700 1 _aAnheim, Mathieu
700 1 _aTranchant, Christine
700 1 _aFrebourg, Thierry
700 1 _aCampion, Dominique
700 1 _aHannequin, Didier
773 0 _tNeurogenetics
_gvol. 15
_gno. 3
_gp. 215-6
856 4 0 _uhttps://doi.org/10.1007/s10048-014-0404-2
_zAvailable from publisher's website
999 _c23773355
_d23773355