| 000 | 01826 a2200565 4500 | ||
|---|---|---|---|
| 005 | 20250518041549.0 | ||
| 264 | 0 | _c20200309 | |
| 008 | 202003s 0 0 eng d | ||
| 022 | _a1098-1004 | ||
| 024 | 7 |
_a10.1002/humu.23817 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aFanis, Pavlos | |
| 245 | 0 | 0 |
_aA novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β-thalassemia major. _h[electronic resource] |
| 260 |
_bHuman mutation _c10 2019 |
||
| 300 |
_a1768-1780 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aBiomarkers |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aErythrocyte Indices |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFetal Hemoglobin _xgenetics |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aKruppel-Like Transcription Factors _xchemistry |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aProtein Conformation |
| 650 | 0 | 4 | _aSeverity of Illness Index |
| 650 | 0 | 4 | _aStructure-Activity Relationship |
| 650 | 0 | 4 | _aSymptom Assessment |
| 650 | 0 | 4 |
_abeta-Globins _xgenetics |
| 650 | 0 | 4 |
_abeta-Thalassemia _xblood |
| 700 | 1 | _aKousiappa, Ioanna | |
| 700 | 1 | _aPhylactides, Marios | |
| 700 | 1 | _aKyrri, Andreani | |
| 700 | 1 | _aHadjigavriel, Michael | |
| 700 | 1 | _aChristou, Soteroula | |
| 700 | 1 | _aSitarou, Maria | |
| 700 | 1 | _aKleanthous, Marina | |
| 773 | 0 |
_tHuman mutation _gvol. 40 _gno. 10 _gp. 1768-1780 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.23817 _zAvailable from publisher's website |
| 999 |
_c29716966 _d29716966 |
||