Volume 43, Issue 6 pp. e294-e297
LETTER TO THE EDITOR

A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next-generation sequencing in a Chinese family

Ru-Qing Zhao

Ru-Qing Zhao

Panyu Maternal and Children Healthcare Hospital, Hexian Memorial Medical Hospital of Panyu District, Guangzhou, China

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Fan Jiang

Fan Jiang

Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou, China

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Jian Li

Jian Li

Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou, China

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Jian-Ying Zhou

Jian-Ying Zhou

Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou, China

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Xue-Wei Tang

Xue-Wei Tang

Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou, China

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Fa-Tao Li

Fa-Tao Li

Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou, China

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Li-Qiong Chen

Li-Qiong Chen

Panyu Maternal and Children Healthcare Hospital, Hexian Memorial Medical Hospital of Panyu District, Guangzhou, China

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Dong-Zhi Li

Corresponding Author

Dong-Zhi Li

Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou, China

Correspondence

Dong-Zhi Li, Guangzhou Women and Children Medical Center, Guangzhou, Guangdong, China.

Email: [email protected]

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First published: 11 May 2021
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CONFLICT OF INTEREST

The authors declare that they have no conflicts of interest.

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