000 01737 a2200493 4500
005 20250516173352.0
264 0 _c20140724
008 201407s 0 0 eng d
022 _a1873-2364
024 7 _a10.1016/j.nmd.2013.09.008
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMastaglia, F L
245 0 0 _aPolymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms.
_h[electronic resource]
260 _bNeuromuscular disorders : NMD
_cDec 2013
300 _a969-74 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAge of Onset
650 0 4 _aAged
650 0 4 _aApolipoproteins E
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Frequency
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aKaplan-Meier Estimate
650 0 4 _aMale
650 0 4 _aMembrane Transport Proteins
_xgenetics
650 0 4 _aMiddle Aged
650 0 4 _aMitochondrial Precursor Protein Import Complex Proteins
650 0 4 _aMyositis, Inclusion Body
_xgenetics
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aTrinucleotide Repeat Expansion
_xgenetics
700 1 _aRojana-udomsart, A
700 1 _aJames, I
700 1 _aNeedham, M
700 1 _aDay, T J
700 1 _aKiers, L
700 1 _aCorbett, J A
700 1 _aSaunders, A M
700 1 _aLutz, M W
700 1 _aRoses, A D
773 0 _tNeuromuscular disorders : NMD
_gvol. 23
_gno. 12
_gp. 969-74
856 4 0 _uhttps://doi.org/10.1016/j.nmd.2013.09.008
_zAvailable from publisher's website
999 _c23150190
_d23150190