000 | 00946 a2200265 4500 | ||
---|---|---|---|
005 | 20250516043059.0 | ||
264 | 0 | _c20111110 | |
008 | 201111s 0 0 eng d | ||
022 | _a1757-790X | ||
024 | 7 |
_a10.1136/bcr.08.2008.0652 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMuglia, Maria | |
245 | 0 | 0 |
_aA novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. _h[electronic resource] |
260 |
_bBMJ case reports _c2009 |
||
500 | _aPublication Type: Journal Article | ||
700 | 1 | _aVazza, Giovanni | |
700 | 1 | _aPatitucci, Alessandra | |
700 | 1 | _aMilani, Micaela | |
700 | 1 | _aPareyson, Davide | |
700 | 1 | _aTaroni, Franco | |
700 | 1 | _aQuattrone, Aldo | |
700 | 1 | _aMostacciuolo, Maria Luisa | |
773 | 0 |
_tBMJ case reports _gvol. 2009 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1136/bcr.08.2008.0652 _zAvailable from publisher's website |
999 |
_c20941092 _d20941092 |