Cerebral aneurysms and kidney disease in a child with microcephalic osteodysplastic primordial dwarfism type II: novel homozygous mutation in the PCNT gene

被引：0
|
作者：
Petraroli, Maddalena [1 ,2 ]
Percesepe, Antonio [3 ]
Piane, Maria [4 ]
Gnocchi, Margherita [1 ,2 ]
Messina, Giulia [1 ,2 ]
Lattanzi, Claudia [1 ,2 ]
D'alvano, Tiziana [1 ,2 ]
Patianna, Viviana Dora [1 ,2 ]
Ormitti, Francesca [5 ]
Esposito, Susanna Maria Roberta [1 ,2 ]
Street, Maria Elisabeth [1 ,2 ]
机构：
[1] Univ Parma, Dept Med & Surg, Unit Paediat, Parma, Italy
[2] P Barilla Childrens Hosp, Parma, Italy
[3] Univ Parma, Med Genet Unit, Parma, Italy
[4] Sapienza Univ Rome, Dept Clin & Mol Med, Rome, Italy
[5] Univ Parma, Radiol Unit, Parma, Italy
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2022年 / 95卷 / SUPPL 2期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P1-532
引用
收藏
页码：322 / 322
页数：1
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