作者：
Arif B,Ekici [1]
;
Thomas,Hackenbeck [2]
;
Vincent,Morinière [3]
;
Andrea,Pannes [4]
;
Maike,Buettner [5]
;
Steffen,Uebe [1]
;
Rolf,Janka [6]
;
Antje,Wiesener [1]
;
Ingo,Hermann [2]
;
Sina,Grupp [2]
;
Martin,Hornberger [7]
;
Tobias B,Huber [8]
;
Nikky,Isbel [9]
;
George,Mangos [10]
;
Stella,McGinn [11]
;
Daniela,Soreth-Rieke [12]
;
Bodo B,Beck [4]
;
Michael,Uder [6]
;
Kerstin,Amann [5]
;
Corinne,Antignac [13]
;
André,Reis [1]
;
Kai-Uwe,Eckardt [14]
;
Michael S,Wiesener [2]
作者单位：
Institute for Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
[1]
1] Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany [2] Nikolaus-Fiebiger-Center of Molecular Medicine, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
[2]
Department of Genetics, Assistance Publique-Hopitaux de Paris, Necker Hospital, Paris, France.
[3]
Institute for Human Genetics, University of Cologne, Cologne, Germany.
[4]
Department of Nephropathology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
[5]
Department of Radiology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
[6]
Department of Nephrology and Hypertension, Hospital of Offenburg, Offenburg, Germany.
[7]
1] Renal Division, University Hospital Freiburg, Freiburg, Germany [2] BIOSS Centre for Biological Signalling Studies, Albert-Ludwigs-University, Freiburg, Germany.
[8]
Department of Renal Medicine, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
[9]
Department of Renal Medicine, St George Clinical School, University of New South Wales, Kogarah, New South Wales, Australia.
[10]
Department of Renal Medicine, Royal North Shore Hospital, Sydney, New South Wales, Australia.
[11]
KfH Nierenzentrum Miesbach, Miesbach, Germany.
[12]
1] Inserm, U983, Necker Hospital, Paris, France [2] Université Paris Descartes, Sorbonne Paris Cité, Institut Imagine, Paris, France.
[13]
Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
[14]
主题词
萎缩(Atrophy);染色体畸变(Chromosome Aberrations);染色体, 人, 1对(Chromosomes, Human, Pair 1);染色体, 人, 16对(Chromosomes, Human, Pair 16);女(雌)性(Female);纤维化(Fibrosis);单倍型(Haplotypes);人类(Humans);肾小管(Kidney Tubules);磁共振成像(Magnetic Resonance Imaging);男(雄)性(Male);黏蛋白-1(Mucin-1);肾炎, 间质性(Nephritis, Interstitial);系谱(Pedigree);科学术语(主题)(Terminology as Topic);尿调节素(Uromodulin)
DOI
10.1038/ki.2014.72
PMID
24670410
发布时间
2014-08-29
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