000 01581 a2200457 4500
005 20250515005224.0
264 0 _c20060302
008 200603s 0 0 eng d
022 _a0960-8966
024 7 _a10.1016/j.nmd.2005.08.008
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPegoraro, Elena
245 0 0 _aCo-segregation of LMNA and PMP22 gene mutations in the same family.
_h[electronic resource]
260 _bNeuromuscular disorders : NMD
_cDec 2005
300 _a858-62 p.
_bdigital
500 _aPublication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aHereditary Sensory and Motor Neuropathy
_xgenetics
650 0 4 _aHumans
650 0 4 _aLamin Type A
_xgenetics
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMuscle, Skeletal
_xpathology
650 0 4 _aMuscular Dystrophies, Limb-Girdle
_xgenetics
650 0 4 _aMutation
650 0 4 _aMyelin Proteins
_xgenetics
650 0 4 _aNeural Conduction
_xphysiology
700 1 _aGavassini, Bruno F
700 1 _aBenedetti, Sara
700 1 _aMenditto, Immacolata
700 1 _aZara, Gabriella
700 1 _aPadoan, Roberta
700 1 _aMostacciuolo, Maria Luisa
700 1 _aFerrari, Maurizio
700 1 _aAngelini, Corrado
773 0 _tNeuromuscular disorders : NMD
_gvol. 15
_gno. 12
_gp. 858-62
856 4 0 _uhttps://doi.org/10.1016/j.nmd.2005.08.008
_zAvailable from publisher's website
999 _c15913072
_d15913072