000 01013 a2200289 4500
005 20250514193626.0
264 0 _c20041221
008 200412s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/wnl.63.1.194
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKamholz, John
245 0 0 _aLate onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene.
_h[electronic resource]
260 _bNeurology
_cJul 2004
300 _a194; author reply 194 p.
_bdigital
500 _aPublication Type: Comment; Letter
650 0 4 _aAmino Acid Sequence
650 0 4 _aAmino Acid Substitution
650 0 4 _aCharcot-Marie-Tooth Disease
_xgenetics
650 0 4 _aCodon
_xgenetics
650 0 4 _aHumans
650 0 4 _aMutation, Missense
650 0 4 _aMyelin P0 Protein
_xchemistry
700 1 _aShy, Michael E
773 0 _tNeurology
_gvol. 63
_gno. 1
_gp. 194; author reply 194
856 4 0 _uhttps://doi.org/10.1212/wnl.63.1.194
_zAvailable from publisher's website
999 _c14952694
_d14952694