Clinical spectrum and prognosis of the atypical polycystic kidney disease caused by monoallelic loss-of-function IFT140 variants

被引：0
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作者：
Zagorec, Nikola [1 ,2 ]
Calamel, Alizee [3 ]
Ars, Elisabet [4 ]
Ong, Albert [5 ]
Halbritter, Jan [6 ]
Audrezet, Marie-Pierre [7 ]
Pillay, Vignesh-Guru [8 ]
Le Meur, Yannick [9 ,10 ]
Sayer, John [11 ]
Cornec-Le Gall, Emilie [7 ,10 ]
机构：
[1] CHR Brest, Brest, France
[2] Dubrava Univ Hosp, Dept Nephrol & Dialysis, Zagreb, Croatia
[3] CHU Brest, Dept Nephrol Hemodialysis & Renal Transplantat, Brest, France
[4] Univ Autonoma Barcelona, Inherited Kidney Disorders, Fundacio Puigvert, Barcelona, Spain
[5] Univ Sheffield, Sheffield Teaching Hosp NHS Fdn Trust, Dept Infect Immun & Cardiovasc Dis, Med Sch,Sheffield Kidney Inst,Acad Nephrol Unit, Sheffield, S Yorkshire, England
[6] Charite Univ Med Berlin, Dept Nephrol & Med Intens Care, Berlin, Germany
[7] Univ Brest, CHU Brest, INSERM, UMR 1078,GGB, Brest, France
[8] Hop Univ Dijon, Dijon, France
[9] Univ Brest, UMR 1227, LBAI, Brest, France
[10] CHRU Brest, Dept Nephrol Hemodialysis & Renal Transplantat, Brest, France
[11] Newcastle Univ, Fac Med Sci, Translat & Clin Res Inst, Newcastle Upon Tyne, Tyne & Wear, England
[12] Genkyst Cohort, Brest, France
来源：
NEPHROLOGY DIALYSIS TRANSPLANTATION | 2024年 / 39卷
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暂无
中图分类号：
R3 [基础医学]; R4 [临床医学];
学科分类号：
1001 ; 1002 ; 100602 ;
摘要：
2613
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页码：I213 / I214
页数：2
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