000 01224 a2200385 4500
005 20250515074410.0
264 0 _c20070803
008 200708s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/01.wnl.0000265820.51075.61
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFabrizi, G M
245 0 0 _aTwo novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease.
_h[electronic resource]
260 _bNeurology
_cJul 2007
300 _a291-5 p.
_bdigital
500 _aPublication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAxons
_xmetabolism
650 0 4 _aCharcot-Marie-Tooth Disease
_xgenetics
650 0 4 _aDynamin II
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aPedigree
700 1 _aFerrarini, M
700 1 _aCavallaro, T
700 1 _aCabrini, I
700 1 _aCerini, R
700 1 _aBertolasi, L
700 1 _aRizzuto, N
773 0 _tNeurology
_gvol. 69
_gno. 3
_gp. 291-5
856 4 0 _uhttps://doi.org/10.1212/01.wnl.0000265820.51075.61
_zAvailable from publisher's website
999 _c17170573
_d17170573