000 01051 a2200301 4500
005 20250513111309.0
264 0 _c19970402
008 199704s 0 0 eng d
022 _a1350-7540
024 7 _a10.1097/00019052-199612000-00014
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMoser, H W
245 0 0 _aPathogenetic mechanisms in peroxisomal disorders.
_h[electronic resource]
260 _bCurrent opinion in neurology
_cDec 1996
300 _a473-6 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aBone Marrow Transplantation
650 0 4 _aDNA Mutational Analysis
650 0 4 _aGenetic Complementation Test
650 0 4 _aGenetic Therapy
650 0 4 _aHumans
650 0 4 _aPeroxisomal Disorders
_xdiagnosis
650 0 4 _aPrognosis
650 0 4 _aSex Chromosome Aberrations
_xgenetics
650 0 4 _aX Chromosome
773 0 _tCurrent opinion in neurology
_gvol. 9
_gno. 6
_gp. 473-6
856 4 0 _uhttps://doi.org/10.1097/00019052-199612000-00014
_zAvailable from publisher's website
999 _c8998419
_d8998419