000 | 01013 a2200289 4500 | ||
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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 |