| 000 | 01597 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250513142053.0 | ||
| 264 | 0 | _c19980507 | |
| 008 | 199805s 0 0 eng d | ||
| 022 | _a0028-3878 | ||
| 024 | 7 |
_a10.1212/wnl.50.4.1105 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTerwindt, G M | |
| 245 | 0 | 0 |
_aVariable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group. _h[electronic resource] |
| 260 |
_bNeurology _cApr 1998 |
||
| 300 |
_a1105-10 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aBrain Chemistry _xgenetics |
| 650 | 0 | 4 |
_aCalcium Channels _xgenetics |
| 650 | 0 | 4 | _aCalcium Channels, N-Type |
| 650 | 0 | 4 |
_aCerebellar Ataxia _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Expression |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHemiplegia _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMigraine Disorders _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aRepetitive Sequences, Nucleic Acid |
| 700 | 1 | _aOphoff, R A | |
| 700 | 1 | _aHaan, J | |
| 700 | 1 | _aVergouwe, M N | |
| 700 | 1 | _avan Eijk, R | |
| 700 | 1 | _aFrants, R R | |
| 700 | 1 | _aFerrari, M D | |
| 773 | 0 |
_tNeurology _gvol. 50 _gno. 4 _gp. 1105-10 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/wnl.50.4.1105 _zAvailable from publisher's website |
| 999 |
_c9533464 _d9533464 |
||