| 000 | 01455 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250517035333.0 | ||
| 264 | 0 | _c20160328 | |
| 008 | 201603s 0 0 eng d | ||
| 022 | _a1933-690X | ||
| 024 | 7 |
_a10.1080/19336896.2015.1054601 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSun, Lin | |
| 245 | 0 | 0 |
_aFamilial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene. _h[electronic resource] |
| 260 |
_bPrion _c2015 |
||
| 300 |
_a228-35 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aBrain _xpathology |
| 650 | 0 | 4 |
_aCodon _xgenetics |
| 650 | 0 | 4 | _aElectroencephalography |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInsomnia, Fatal Familial _xgenetics |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMethionine _xgenetics |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPrions _xgenetics |
| 700 | 1 | _aLi, Xia | |
| 700 | 1 | _aLin, Xiang | |
| 700 | 1 | _aYan, Feng | |
| 700 | 1 | _aChen, Kathryn | |
| 700 | 1 | _aXiao, Shifu | |
| 773 | 0 |
_tPrion _gvol. 9 _gno. 3 _gp. 228-35 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1080/19336896.2015.1054601 _zAvailable from publisher's website |
| 999 |
_c24981621 _d24981621 |
||