Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families

被引：0

作者：

Mohamed H. Al-Hamed

Nada Alsahan

Sarah J. Rice

Noel Edwards

Eman Nooreddeen

Maha Alotaibi

Wesam Kurdi

Maha Alnemer

Naderah Altaleb

Wafa Ali

Nouf Al-Numair

Najd Almejaish

John A. Sayer

Faiqa Imtiaz

机构：

[1] King Faisal Specialist Hospital and Research Centre,Department of Genetics

[2] King Faisal Specialist Hospital and Research Centre,Department of Obstetrics and Gynecology

[3] Newcastle University,Institute of Genetic Medicine

[4] National Guard Hospital,Paediatric Nephrology Department

[5] King Saud Medical City,Division of Genetics & Metabolic

[6] NIHR Newcastle Biomedical Research Centre,undefined

来源：

Pediatric Nephrology | 2019年 / 34卷

关键词：

ADPKD; PKD1; Biallelic mutations; Molecular genetics; Consanguinity;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：1615 / 1623

页数：8

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[1] Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families
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[J]. PEDIATRIC NEPHROLOGY, 2019, 34 (09) : 1615 - 1623
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