Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing

Xiaoyun HuDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaView further author information

Tao HuangDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaCorrespondence[email protected]
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Yun LiuDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaView further author information

Lina ZhangDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaView further author information

Li ZhuDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaView further author information

Xiaohong PengDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaView further author information

Sufang ZhangDepartment of Pediatrics, The First Affiliated Hospital of Nanchang University, Nanchang, People’s Republic of ChinaView further author information

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Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing

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Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing

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