Danhua Liu

3PUBLICATIONS
14CO-AUTHORS
Gene mappingEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Publications (3)

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|Jul 14, 2021
Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.

Jinying Li, Hongen Xu, Jianfeng Sun

|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

Bei Chen

2 joint publications

Yongan Tian

2 joint publications

Wenxue Tang

1 joint publications

Rongqun Zhai

1 joint publications

Haifeng Feng

1 joint publications

Jinying Li

1 joint publications

Jianfeng Sun

1 joint publications

Yaping Qin

1 joint publications

Ruijun Li

Frequent Collaborators

3 joint publications

Hongen Xu

2 joint publications

Bei Chen

2 joint publications

Yongan Tian

2 joint publications

Wenxue Tang

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