| 000 | 01320 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250516042901.0 | ||
| 264 | 0 | _c20120117 | |
| 008 | 201201s 0 0 eng d | ||
| 022 | _a1098-1004 | ||
| 024 | 7 |
_a10.1002/humu.21547 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWolf, Andreas | |
| 245 | 0 | 0 |
_aSingle base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease. _h[electronic resource] |
| 260 |
_bHuman mutation _cOct 2011 |
||
| 300 |
_a1137-43 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _a5' Flanking Region |
| 650 | 0 | 4 | _aCodon, Initiator |
| 650 | 0 | 4 | _aConsensus Sequence |
| 650 | 0 | 4 | _aDatabases, Genetic |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMutation Rate |
| 650 | 0 | 4 | _aOpen Reading Frames |
| 650 | 0 | 4 |
_aPeptide Chain Initiation, Translational _xgenetics |
| 650 | 0 | 4 | _aPoint Mutation |
| 700 | 1 | _aCaliebe, Amke | |
| 700 | 1 | _aThomas, Nick S T | |
| 700 | 1 | _aBall, Edward V | |
| 700 | 1 | _aMort, Matthew | |
| 700 | 1 | _aStenson, Peter D | |
| 700 | 1 | _aKrawczak, Michael | |
| 700 | 1 | _aCooper, David N | |
| 773 | 0 |
_tHuman mutation _gvol. 32 _gno. 10 _gp. 1137-43 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.21547 _zAvailable from publisher's website |
| 999 |
_c20936457 _d20936457 |
||