000 01770 a2200505 4500
005 20250515195346.0
264 0 _c20100812
008 201008s 0 0 eng d
022 _a1432-1459
024 7 _a10.1007/s00415-009-5401-2
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHuang, Jia
245 0 0 _aCopy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease.
_h[electronic resource]
260 _bJournal of neurology
_cMay 2010
300 _a735-41 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aCharcot-Marie-Tooth Disease
_xetiology
650 0 4 _aChromosomes, Human, Pair 17
650 0 4 _aDNA Copy Number Variations
650 0 4 _aExons
650 0 4 _aFemale
650 0 4 _aGene Duplication
650 0 4 _aGuanine Nucleotide Exchange Factors
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMicroarray Analysis
_xmethods
650 0 4 _aMyelin Proteins
_xgenetics
650 0 4 _aNucleic Acid Hybridization
_xmethods
650 0 4 _aPeripheral Nervous System Diseases
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aProtein Tyrosine Phosphatases, Non-Receptor
_xgenetics
650 0 4 _aReproducibility of Results
650 0 4 _aRho Guanine Nucleotide Exchange Factors
650 0 4 _aSequence Analysis, DNA
700 1 _aWu, Xingyao
700 1 _aMontenegro, Gladys
700 1 _aPrice, Justin
700 1 _aWang, Gaofeng
700 1 _aVance, Jeffery M
700 1 _aShy, Michael E
700 1 _aZüchner, Stephan
773 0 _tJournal of neurology
_gvol. 257
_gno. 5
_gp. 735-41
856 4 0 _uhttps://doi.org/10.1007/s00415-009-5401-2
_zAvailable from publisher's website
999 _c19333329
_d19333329