Qin Gu

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Neurology and neuromuscular diseases
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Publications (1)

|Aug 10, 2023
Whole Exome Sequencing Identified two Novel Truncation Mutations in the CTNNB1 Gene Associated with Neurodevelopmental Disorder, Language Dysfunction, and Microcephaly in Chinese Children.

Yongchun Ji, Qin Xia, Hewei Zhang

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