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Bei Chen

3PUBLICATIONS

9CO-AUTHORS

Gene mappingEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases

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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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Frequent Collaborators

3 joint publications

Hongen Xu

2 joint publications

Danhua Liu

1 joint publications

Rongqun Zhai

1 joint publications

Haifeng Feng

1 joint publications

Yongan Tian

1 joint publications

Wenxue Tang

1 joint publications

Peipei Li

1 joint publications

Ting Zhang

1 joint publications

Xingle Zhao

Frequent Collaborators

3 joint publications

Hongen Xu

2 joint publications

Danhua Liu

1 joint publications

Rongqun Zhai

1 joint publications

Haifeng Feng

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