000			02208 a2200601 4500
005			20250514075220.0
264		0	_c20031007
008			200310s 0 0 eng d
022			_a0960-8966
024	7		_a10.1016/s0960-8966(03)00070-1 _2doi
040			_aNLM _beng _cNLM
100	1		_aWatts, Giles D J
245	0	0	_aClinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes. _h[electronic resource]
260			_bNeuromuscular disorders : NMD _cSep 2003
300			_a559-67 p. _bdigital
500			_aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aAged
650	0	4	_aAmino Acid Sequence
650	0	4	_aBase Sequence
650	0	4	_aCaenorhabditis elegans Proteins
650	0	4	_aCarbohydrate Epimerases _xgenetics
650	0	4	_aCarrier Proteins _xgenetics
650	0	4	_aChromosomes, Human, Pair 9
650	0	4	_aDNA Mutational Analysis _xmethods
650	0	4	_aDNA, Recombinant
650	0	4	_aDementia _xcomplications
650	0	4	_aExons
650	0	4	_aGenetic Heterogeneity
650	0	4	_aGenetic Linkage
650	0	4	_aGenetic Markers
650	0	4	_aHumans
650	0	4	_aMiddle Aged
650	0	4	_aMolecular Sequence Data
650	0	4	_aMuscular Dystrophies _xcomplications
650	0	4	_aMutation
650	0	4	_aMyositis, Inclusion Body _xcomplications
650	0	4	_aNADH, NADPH Oxidoreductases _xgenetics
650	0	4	_aNuclear Proteins _xgenetics
650	0	4	_aOsteitis Deformans _xcomplications
650	0	4	_aPedigree
650	0	4	_aPhosphotransferases (Alcohol Group Acceptor) _xgenetics
650	0	4	_aRNA, Messenger _xbiosynthesis
650	0	4	_aReverse Transcriptase Polymerase Chain Reaction _xmethods
650	0	4	_aTropomyosin _xgenetics
700	1		_aThorne, M
700	1		_aKovach, M J
700	1		_aPestronk, A
700	1		_aKimonis, Virginia E
773	0		_tNeuromuscular disorders : NMD _gvol. 13 _gno. 7-8 _gp. 559-67
856	4	0	_uhttps://doi.org/10.1016/s0960-8966(03)00070-1 _zAvailable from publisher's website
999			_c12694722 _d12694722