000 01138 a2200325 4500
005 20250514020328.0
264 0 _c20020520
008 200205s 0 0 eng d
022 _a1084-9521
024 7 _a10.1006/scdb.2001.0278
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aZeviani, M
245 0 0 _aThe expanding spectrum of nuclear gene mutations in mitochondrial disorders.
_h[electronic resource]
260 _bSeminars in cell & developmental biology
_cDec 2001
300 _a407-16 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAnimals
650 0 4 _aChild
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMice
650 0 4 _aMitochondrial Diseases
_xgenetics
650 0 4 _aModels, Animal
650 0 4 _aMutation
650 0 4 _aNeurodegenerative Diseases
_xgenetics
650 0 4 _aOxidative Phosphorylation
773 0 _tSeminars in cell & developmental biology
_gvol. 12
_gno. 6
_gp. 407-16
856 4 0 _uhttps://doi.org/10.1006/scdb.2001.0278
_zAvailable from publisher's website
999 _c11648899
_d11648899