Bei Chen
3PUBLICATIONS
9CO-AUTHORS
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Publications (3)
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|Oct 08, 2025
Atypical phenotypic characteristics, mutation analysis and treatment in a family of riboflavin transporter deficiency caused by SLC52A3 variants.Peipei Li, Ting Zhang, Hongen Xu
|Jun 25, 2021
Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.Yongan Tian, Hongen Xu, Danhua Liu
|Jan 11, 2021
Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families.Rongqun Zhai, Haifeng Feng, Qingli Li
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