000 01150 a2200325 4500
005 20250516153859.0
264 0 _c20140207
008 201402s 0 0 eng d
022 _a0168-9525
024 7 _a10.1016/j.tig.2013.05.005
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFarrar, G Jane
245 0 0 _aMitochondrial disorders: aetiologies, models systems, and candidate therapies.
_h[electronic resource]
260 _bTrends in genetics : TIG
_cAug 2013
300 _a488-97 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAnimals
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aDisease Models, Animal
650 0 4 _aGenetic Therapy
650 0 4 _aHumans
650 0 4 _aMitochondria
_xgenetics
650 0 4 _aMutation
650 0 4 _aOptic Atrophy, Hereditary, Leber
_xgenetics
700 1 _aChadderton, Naomi
700 1 _aKenna, Paul F
700 1 _aMillington-Ward, Sophia
773 0 _tTrends in genetics : TIG
_gvol. 29
_gno. 8
_gp. 488-97
856 4 0 _uhttps://doi.org/10.1016/j.tig.2013.05.005
_zAvailable from publisher's website
999 _c22825921
_d22825921