000 01457 a2200421 4500
005 20250515031140.0
264 0 _c20070118
008 200701s 0 0 eng d
022 _a0025-7931
024 7 _a10.1159/000093818
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMainz, J
245 0 0 _aCystic fibrosis in 65- and 67-year-old siblings. Clinical feature and nasal potential difference measurement in patients with genotypes F508del and 2789+5G-->A.
_h[electronic resource]
260 _bRespiration; international review of thoracic diseases
_c2006
300 _a698-704 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAged
650 0 4 _aAmiloride
650 0 4 _aChlorides
_xanalysis
650 0 4 _aCystic Fibrosis
_xdiagnosis
650 0 4 _aCystic Fibrosis Transmembrane Conductance Regulator
_xgenetics
650 0 4 _aGenetic Carrier Screening
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMembrane Potentials
650 0 4 _aNasal Mucosa
_xphysiology
650 0 4 _aPhenotype
650 0 4 _aSiblings
650 0 4 _aSweat
_xchemistry
700 1 _aHammer, U
700 1 _aRokahr, C
700 1 _aHubler, A
700 1 _aZintl, F
700 1 _aBallmann, M
773 0 _tRespiration; international review of thoracic diseases
_gvol. 73
_gno. 5
_gp. 698-704
856 4 0 _uhttps://doi.org/10.1159/000093818
_zAvailable from publisher's website
999 _c16359078
_d16359078