000 01518 a2200445 4500
005 20250514182815.0
264 0 _c20040816
008 200408s 0 0 eng d
022 _a1061-4036
024 7 _a10.1038/ng1332
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWatts, Giles D J
245 0 0 _aInclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.
_h[electronic resource]
260 _bNature genetics
_cApr 2004
300 _a377-81 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdenosine Triphosphatases
650 0 4 _aCell Cycle Proteins
_xgenetics
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 9
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aImmunohistochemistry
650 0 4 _aMale
650 0 4 _aMuscular Diseases
_xgenetics
650 0 4 _aMutation
650 0 4 _aOsteitis Deformans
_xgenetics
650 0 4 _aPedigree
650 0 4 _aValosin Containing Protein
700 1 _aWymer, Jill
700 1 _aKovach, Margaret J
700 1 _aMehta, Sarju G
700 1 _aMumm, Steven
700 1 _aDarvish, Daniel
700 1 _aPestronk, Alan
700 1 _aWhyte, Michael P
700 1 _aKimonis, Virginia E
773 0 _tNature genetics
_gvol. 36
_gno. 4
_gp. 377-81
856 4 0 _uhttps://doi.org/10.1038/ng1332
_zAvailable from publisher's website
999 _c14752079
_d14752079