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

页码：322 / 322

页数：1

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