000 01089 a2200325 4500
005 20250511200502.0
264 0 _c19910911
008 199109s 0 0 eng d
022 _a0140-6736
024 7 _a10.1016/0140-6736(91)91090-h
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBerkovic, S F
245 0 0 _aClinical spectrum of mitochondrial DNA mutation at base pair 8344.
_h[electronic resource]
260 _bLancet (London, England)
_cAug 1991
300 _a457 p.
_bdigital
500 _aPublication Type: Comment; Letter
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aEpilepsies, Myoclonic
_xgenetics
650 0 4 _aHumans
650 0 4 _aMutation
_xgenetics
650 0 4 _aRNA, Transfer, Lys
_xgenetics
700 1 _aShoubridge, E A
700 1 _aAndermann, F
700 1 _aAndermann, E
700 1 _aCarpenter, S
700 1 _aKarpati, G
773 0 _tLancet (London, England)
_gvol. 338
_gno. 8764
_gp. 457
856 4 0 _uhttps://doi.org/10.1016/0140-6736(91)91090-h
_zAvailable from publisher's website
999 _c1684540
_d1684540