000 01211 a2200361 4500
005 20250512084003.0
264 0 _c19850826
008 198508s 0 0 eng d
022 _a0001-656X
024 7 _a10.1111/j.1651-2227.1985.tb11046.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChitayat, D
245 0 0 _aPseudohypoaldosteronism in a female infant and her family: diversity of clinical expression and mode of inheritance.
_h[electronic resource]
260 _bActa paediatrica Scandinavica
_cJul 1985
300 _a619-22 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aAldosterone
_xmetabolism
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aRenal Tubular Transport, Inborn Errors
_xgenetics
650 0 4 _aSodium Chloride
_xurine
650 0 4 _aSyndrome
700 1 _aSpirer, Z
700 1 _aAyalon, D
700 1 _aGolander, A
773 0 _tActa paediatrica Scandinavica
_gvol. 74
_gno. 4
_gp. 619-22
856 4 0 _uhttps://doi.org/10.1111/j.1651-2227.1985.tb11046.x
_zAvailable from publisher's website
999 _c4030620
_d4030620