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 |