000 01167 a2200337 4500
005 20250513040723.0
264 0 _c19950504
008 199505s 0 0 eng d
022 _a0300-5127
024 7 _a10.1042/bst0220996
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchapira, A H
245 0 0 _aInborn and induced defects of the mitochondrial respiratory chain.
_h[electronic resource]
260 _bBiochemical Society transactions
_cNov 1994
300 _a996-1001 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAnimals
650 0 4 _aBrain Diseases, Metabolic
_xgenetics
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aHumans
650 0 4 _aMetabolism, Inborn Errors
_xgenetics
650 0 4 _aMitochondria
_xmetabolism
650 0 4 _aMitochondrial Encephalomyopathies
_xgenetics
650 0 4 _aMutation
650 0 4 _aOxygen Consumption
650 0 4 _aPoint Mutation
650 0 4 _aSequence Deletion
700 1 _aCooper, J M
773 0 _tBiochemical Society transactions
_gvol. 22
_gno. 4
_gp. 996-1001
856 4 0 _uhttps://doi.org/10.1042/bst0220996
_zAvailable from publisher's website
999 _c7697910
_d7697910