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The Journal of Maternal-Fetal & Neonatal Medicine Volume 34, 2021 - Issue 20
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Original Articles

Whole exome sequencing identifies c.963T > A and c.492 + 1G > A mutations in REN responsible for autosomal recessive renal tubular dysgenesis

Guannan Hea Department of Ultrasound, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaView further author information
,
Jing Zhaoa Department of Ultrasound, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaView further author information
,
Xueyan Wangb Department of Prenatal Diagnosis, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaCorrespondence[email protected]
View further author information
,
Shengmei Lic Department of Gynecology, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaView further author information
,
Shengfang Qinb Department of Prenatal Diagnosis, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaView further author information
,
Ximin Chenb Department of Prenatal Diagnosis, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaView further author information
&
Na Xib Department of Prenatal Diagnosis, Women and Children’s Hospital of Sichuan Province, Chengdu, ChinaView further author information
 show all
Pages 3300-3305 | Received 12 Sep 2019, Accepted 17 Oct 2019, Published online: 17 Nov 2019

References

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