| 000 | 01019 a2200277 4500 | ||
|---|---|---|---|
| 005 | 20250518034041.0 | ||
| 264 | 0 | _c20190610 | |
| 008 | 201906s 0 0 eng d | ||
| 022 | _a1873-2933 | ||
| 024 | 7 |
_a10.1016/j.clinbiochem.2019.04.008 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aXu, Jing | |
| 245 | 0 | 0 |
_aIdentification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. _h[electronic resource] |
| 260 |
_bClinical biochemistry _cJun 2019 |
||
| 300 |
_a44-49 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAdrenal Hyperplasia, Congenital _xgenetics |
| 650 | 0 | 4 |
_aAsian People _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPseudogenes _xgenetics |
| 650 | 0 | 4 | _aRetrospective Studies |
| 700 | 1 | _aLi, Pin | |
| 773 | 0 |
_tClinical biochemistry _gvol. 68 _gp. 44-49 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.clinbiochem.2019.04.008 _zAvailable from publisher's website |
| 999 |
_c29598771 _d29598771 |
||