| 000 | 01740 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250518050931.0 | ||
| 264 | 0 | _c20200212 | |
| 008 | 202002s 0 0 eng d | ||
| 022 | _a2191-0251 | ||
| 024 | 7 |
_a10.1515/jpem-2018-0538 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGopal-Kothandapani, Jaya Sujatha | |
| 245 | 0 | 0 |
_aPhenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1. _h[electronic resource] |
| 260 |
_bJournal of pediatric endocrinology & metabolism : JPEM _cSep 2019 |
||
| 300 |
_a959-967 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAldosterone _xblood |
| 650 | 0 | 4 |
_aBiomarkers _xanalysis |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCross-Sectional Studies |
| 650 | 0 | 4 |
_aEpithelial Sodium Channels _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFollow-Up Studies |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPrognosis |
| 650 | 0 | 4 |
_aPseudohypoaldosteronism _xclassification |
| 650 | 0 | 4 |
_aReceptors, Mineralocorticoid _xgenetics |
| 700 | 1 | _aDoshi, Arpan B | |
| 700 | 1 | _aSmith, Kath | |
| 700 | 1 | _aChristian, Martin | |
| 700 | 1 | _aMushtaq, Talat | |
| 700 | 1 | _aBanerjee, I | |
| 700 | 1 | _aPadidela, Raja | |
| 700 | 1 | _aRamakrishnan, Renuka | |
| 700 | 1 | _aOwen, Catherine | |
| 700 | 1 | _aCheetham, Timothy | |
| 700 | 1 | _aDimitri, Paul | |
| 773 | 0 |
_tJournal of pediatric endocrinology & metabolism : JPEM _gvol. 32 _gno. 9 _gp. 959-967 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1515/jpem-2018-0538 _zAvailable from publisher's website |
| 999 |
_c29897327 _d29897327 |
||