| 000 | 01357 a2200385 4500 | ||
|---|---|---|---|
| 005 | 20250515144807.0 | ||
| 264 | 0 | _c20090324 | |
| 008 | 200903s 0 0 eng d | ||
| 022 | _a1434-6621 | ||
| 024 | 7 |
_a10.1515/CCLM.2008.339 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAbid, Fatima | |
| 245 | 0 | 0 |
_aCYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. _h[electronic resource] |
| 260 |
_bClinical chemistry and laboratory medicine _c2008 |
||
| 300 |
_a1707-13 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAdrenal Hyperplasia, Congenital _xgenetics |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMorocco |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aSteroid 21-Hydroxylase _xgenetics |
| 700 | 1 | _aTardy, Véronique | |
| 700 | 1 | _aGaouzi, Ahmed | |
| 700 | 1 | _aEl Hessni, Aboubaker | |
| 700 | 1 | _aMorel, Yves | |
| 700 | 1 | _aChabraoui, Layachi | |
| 773 | 0 |
_tClinical chemistry and laboratory medicine _gvol. 46 _gno. 12 _gp. 1707-13 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1515/CCLM.2008.339 _zAvailable from publisher's website |
| 999 |
_c18435349 _d18435349 |
||