| 000 | 01469 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250513232228.0 | ||
| 264 | 0 | _c20010614 | |
| 008 | 200106s 0 0 eng d | ||
| 022 | _a0885-3185 | ||
| 024 | 7 |
_a10.1002/1531-8257(200101)16:1<106::aid-mds1022>3.0.co;2-7 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGrimes, D A | |
| 245 | 0 | 0 |
_aInherited myoclonus-dystonia: evidence supporting genetic heterogeneity. _h[electronic resource] |
| 260 |
_bMovement disorders : official journal of the Movement Disorder Society _cJan 2001 |
||
| 300 |
_a106-10 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 11 _xgenetics |
| 650 | 0 | 4 |
_aDystonic Disorders _xcomplications |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMyoclonus _xcomplications |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPoint Mutation _xgenetics |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 650 | 0 | 4 |
_aReceptors, Dopamine D2 _xgenetics |
| 700 | 1 | _aBulman, D | |
| 700 | 1 | _aGeorge-Hyslop, P S | |
| 700 | 1 | _aLang, A E | |
| 773 | 0 |
_tMovement disorders : official journal of the Movement Disorder Society _gvol. 16 _gno. 1 _gp. 106-10 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/1531-8257(200101)16:1<106::aid-mds1022>3.0.co;2-7 _zAvailable from publisher's website |
| 999 |
_c11153455 _d11153455 |
||