000 01423 a2200397 4500
005 20250515095743.0
264 0 _c20080123
008 200801s 0 0 eng d
022 _a0317-1671
024 7 _a10.1017/s0317167100007290
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBouhouche, Ahmed
245 0 0 _aA novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.
_h[electronic resource]
260 _bThe Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
_cNov 2007
300 _a421-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAge of Onset
650 0 4 _aAmino Acid Sequence
650 0 4 _aCharcot-Marie-Tooth Disease
_xgenetics
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMorocco
_xepidemiology
650 0 4 _aMutation
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aPedigree
700 1 _aBirouk, Nazha
700 1 _aBenomar, Ali
700 1 _aOuazzani, Reda
700 1 _aChkili, Taïeb
700 1 _aYahyaoui, Mohamed
773 0 _tThe Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
_gvol. 34
_gno. 4
_gp. 421-6
856 4 0 _uhttps://doi.org/10.1017/s0317167100007290
_zAvailable from publisher's website
999 _c17576506
_d17576506