000 | 01975 a2200637 4500 | ||
---|---|---|---|
005 | 20250514190737.0 | ||
264 | 0 | _c20041026 | |
008 | 200410s 0 0 eng d | ||
022 | _a1526-632X | ||
024 | 7 |
_a10.1212/01.wnl.0000127310.11526.fd _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aJurkat-Rott, K | |
245 | 0 | 0 |
_aVariability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants. _h[electronic resource] |
260 |
_bNeurology _cMay 2004 |
||
300 |
_a1857-61 p. _bdigital |
||
500 | _aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAged |
650 | 0 | 4 | _aAged, 80 and over |
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 | _aAmino Acid Substitution |
650 | 0 | 4 |
_aComa _xgenetics |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aEpilepsy _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenetic Predisposition to Disease |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 |
_aHemiplegia _xenzymology |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 |
_aMigraine Disorders _xenzymology |
650 | 0 | 4 | _aModels, Molecular |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aPenetrance |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aPoint Mutation |
650 | 0 | 4 | _aRecurrence |
650 | 0 | 4 | _aSequence Alignment |
650 | 0 | 4 | _aSequence Homology, Amino Acid |
650 | 0 | 4 |
_aSodium-Potassium-Exchanging ATPase _xchemistry |
700 | 1 | _aFreilinger, T | |
700 | 1 | _aDreier, J P | |
700 | 1 | _aHerzog, J | |
700 | 1 | _aGöbel, H | |
700 | 1 | _aPetzold, G C | |
700 | 1 | _aMontagna, P | |
700 | 1 | _aGasser, T | |
700 | 1 | _aLehmann-Horn, F | |
700 | 1 | _aDichgans, M | |
773 | 0 |
_tNeurology _gvol. 62 _gno. 10 _gp. 1857-61 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1212/01.wnl.0000127310.11526.fd _zAvailable from publisher's website |
999 |
_c14867925 _d14867925 |