| 000 | 01415 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250516220853.0 | ||
| 264 | 0 | _c20150903 | |
| 008 | 201509s 0 0 eng d | ||
| 022 | _a1365-2265 | ||
| 024 | 7 |
_a10.1111/cen.12526 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBarbaro, Michela | |
| 245 | 0 | 0 |
_aIn vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia. _h[electronic resource] |
| 260 |
_bClinical endocrinology _cJan 2015 |
||
| 300 |
_a37-44 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aAdrenal Hyperplasia, Congenital _xgenetics |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Vitro Techniques |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSteroid 21-Hydroxylase _xgenetics |
| 700 | 1 | _aSoardi, Fernanda C | |
| 700 | 1 | _aÖstberg, Linus J | |
| 700 | 1 | _aPersson, Bengt | |
| 700 | 1 | _ade Mello, Maricilda Palandi | |
| 700 | 1 | _aWedell, Anna | |
| 700 | 1 | _aLajic, Svetlana | |
| 773 | 0 |
_tClinical endocrinology _gvol. 82 _gno. 1 _gp. 37-44 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/cen.12526 _zAvailable from publisher's website |
| 999 |
_c23941977 _d23941977 |
||