Molecular spectrum of genetic anomalies in pediatric patients with early onset of renal cystic disease

被引：0
|
作者：
Bracciama, Valeria [1 ,2 ]
Bucchino, Laura [3 ]
Carli, Diana [1 ,2 ]
Solito, Arianna [3 ]
Faini, Angelo Corso [1 ,2 ]
Kalantari, Silvia [1 ,2 ]
del Prever, Giulia Margherita Brach [1 ,2 ]
Mioli, Fiorenza [1 ,2 ]
Scolari, Caterina [4 ]
Amoroso, Antonio [1 ,2 ]
Vaisitti, Tiziana [1 ,2 ]
Peruzzi, Licia [3 ]
Deaglio, Silvia [1 ,2 ]
机构：
[1] AOU Citta Salute Sci, Transplant Reg Ctr Piedmont Immunogenet & Transpl, Turin, Italy
[2] Univ Turin, Dept Med Sci, Turin, Italy
[3] Regina Margherita Childrens Hosp, Nephrol Dialysis & Transplantat, Turin, Italy
[4] Turin Univ, Turin, Italy
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P04.023.C
引用
收藏
页码：390 / 391
页数：2
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