| 000 | 01671 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250513215224.0 | ||
| 264 | 0 | _c20000828 | |
| 008 | 200008s 0 0 eng d | ||
| 022 | _a1061-4036 | ||
| 024 | 7 |
_a10.1038/78085 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDelépine, M | |
| 245 | 0 | 0 |
_aEIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. _h[electronic resource] |
| 260 |
_bNature genetics _cAug 2000 |
||
| 300 |
_a406-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aDNA _xchemistry |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aDiabetes Mellitus, Type 1 |
| 650 | 0 | 4 |
_aEpiphyses _xabnormalities |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aGrowth Disorders |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMicrosatellite Repeats |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aSequence Homology, Amino Acid |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 |
_aeIF-2 Kinase _xgenetics |
| 700 | 1 | _aNicolino, M | |
| 700 | 1 | _aBarrett, T | |
| 700 | 1 | _aGolamaully, M | |
| 700 | 1 | _aLathrop, G M | |
| 700 | 1 | _aJulier, C | |
| 773 | 0 |
_tNature genetics _gvol. 25 _gno. 4 _gp. 406-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/78085 _zAvailable from publisher's website |
| 999 |
_c10881106 _d10881106 |
||