| 000 | 01470 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250513141922.0 | ||
| 264 | 0 | _c19980506 | |
| 008 | 199805s 0 0 eng d | ||
| 022 | _a0003-9942 | ||
| 024 | 7 |
_a10.1001/archneur.55.4.554 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKori, A A | |
| 245 | 0 | 0 |
_aPendular nystagmus in patients with peroxisomal assembly disorder. _h[electronic resource] |
| 260 |
_bArchives of neurology _cApr 1998 |
||
| 300 |
_a554-8 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aEye Movements _xphysiology |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Recessive |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aNystagmus, Pathologic _xgenetics |
| 650 | 0 | 4 |
_aOptic Atrophy _xgenetics |
| 650 | 0 | 4 |
_aPeroxisomal Disorders _xgenetics |
| 650 | 0 | 4 | _aVision Screening |
| 700 | 1 | _aRobin, N H | |
| 700 | 1 | _aJacobs, J B | |
| 700 | 1 | _aErchul, D M | |
| 700 | 1 | _aZaidat, O O | |
| 700 | 1 | _aRemler, B F | |
| 700 | 1 | _aAverbuch-Heller, L | |
| 700 | 1 | _aDell'Osso, L F | |
| 700 | 1 | _aLeigh, R J | |
| 700 | 1 | _aZinn, A B | |
| 773 | 0 |
_tArchives of neurology _gvol. 55 _gno. 4 _gp. 554-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1001/archneur.55.4.554 _zAvailable from publisher's website |
| 999 |
_c9529068 _d9529068 |
||