000 01173 a2200349 4500
005 20250516080201.0
264 0 _c20130705
008 201307s 0 0 eng d
022 _a1399-0004
024 7 _a10.1111/j.1399-0004.2012.01849.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTsiakkis, D
245 0 0 _aGenotype-phenotype correlation in X-linked Alport syndrome patients carrying missense mutations in the collagenous domain of COL4A5.
_h[electronic resource]
260 _bClinical genetics
_cSep 2012
300 _a297-9 p.
_bdigital
500 _aPublication Type: Letter
650 0 4 _aCollagen Type IV
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Association Studies
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation, Missense
650 0 4 _aNephritis, Hereditary
_xgenetics
650 0 4 _aRegression Analysis
700 1 _aPieri, M
700 1 _aKoupepidou, P
700 1 _aDemosthenous, P
700 1 _aPanayidou, K
700 1 _aDeltas, C
773 0 _tClinical genetics
_gvol. 82
_gno. 3
_gp. 297-9
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.2012.01849.x
_zAvailable from publisher's website
999 _c21546256
_d21546256