000 01390 a2200409 4500
005 20250517035955.0
264 0 _c20160126
008 201601s 0 0 eng d
022 _a1531-8249
024 7 _a10.1002/ana.24464
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMorel, Godelieve
245 0 0 _aCHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy.
_h[electronic resource]
260 _bAnnals of neurology
_cNov 2015
300 _a831 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't; Comment
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMitochondrial Proteins
_xgenetics
650 0 4 _aMuscular Atrophy, Spinal
_xgenetics
650 0 4 _aMutation
_xgenetics
700 1 _aRouzier, Cécile
700 1 _aChaussenot, Annabelle
700 1 _aAit-El-Mkadem, Samira
700 1 _aBannwarth, Sylvie
700 1 _aGenin, Emmanuelle C
700 1 _aAugé, Gaëlle
700 1 _aChabrol, Brigitte
700 1 _aPouget, Jean
700 1 _aSoriani, Marie Hélène
700 1 _aSacconi, Sabrina
700 1 _aPaquis-Flucklinger, Véronique
773 0 _tAnnals of neurology
_gvol. 78
_gno. 5
_gp. 831
856 4 0 _uhttps://doi.org/10.1002/ana.24464
_zAvailable from publisher's website
999 _c25001921
_d25001921