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]
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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

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

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

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