000 | 01794 a2200553 4500 | ||
---|---|---|---|
005 | 20250513082411.0 | ||
264 | 0 | _c19930624 | |
008 | 199306s 0 0 eng d | ||
022 | _a0364-5134 | ||
024 | 7 |
_a10.1002/ana.410330616 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMatthews, P M | |
245 | 0 | 0 |
_aMolecular genetic characterization of an X-linked form of Leigh's syndrome. _h[electronic resource] |
260 |
_bAnnals of neurology _cJun 1993 |
||
300 |
_a652-5 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 | _aAspartic Acid |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 |
_aBrain Stem _xpathology |
650 | 0 | 4 | _aCells, Cultured |
650 | 0 | 4 | _aCesarean Section |
650 | 0 | 4 |
_aCitrate (si)-Synthase _xmetabolism |
650 | 0 | 4 |
_aDNA _xgenetics |
650 | 0 | 4 | _aExons |
650 | 0 | 4 |
_aFibroblasts _xpathology |
650 | 0 | 4 | _aGestational Age |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 |
_aLeigh Disease _xgenetics |
650 | 0 | 4 |
_aLeukocytes _xphysiology |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMitochondria, Heart _xenzymology |
650 | 0 | 4 |
_aMitochondria, Liver _xenzymology |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aNecrosis |
650 | 0 | 4 | _aOligodeoxyribonucleotides |
650 | 0 | 4 | _aPoint Mutation |
650 | 0 | 4 |
_aPyruvate Dehydrogenase Complex _xgenetics |
650 | 0 | 4 |
_aSkin _xpathology |
650 | 0 | 4 | _aX Chromosome |
700 | 1 | _aMarchington, D R | |
700 | 1 | _aSquier, M | |
700 | 1 | _aLand, J | |
700 | 1 | _aBrown, R M | |
700 | 1 | _aBrown, G K | |
773 | 0 |
_tAnnals of neurology _gvol. 33 _gno. 6 _gp. 652-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/ana.410330616 _zAvailable from publisher's website |
999 |
_c8498118 _d8498118 |