Pengfei Lin

11PUBLICATIONS
7CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsNeurology and neuromuscular diseasesGene mappingGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)
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Publications (11)

|Jun 28, 2026
Activation of cryptic donor splice site due to an exonic MYPN variant in congenital myopathy.

|Sep 11, 2025
CSF Aβ, Tau, Axonal, Synaptic, Glial, Neural, and Inflammatory Biomarkers in Patients With Sporadic Amyotrophic Lateral Sclerosis.

Yujing Chen, Sujuan Sun, Zetai Bai

|Aug 16, 2025
Somatic and germinal mosaicism of a canonical splicing variant causing limb-girdle muscular dystrophy type 1B.

Guangyu Wang, Yaru Wang, Dandan Zhao

|Apr 07, 2025
RNA Mis-Splicing Effects of Noncanonical Splicing Variants in Limb-Girdle Muscular Dystrophy Type R1/2A.

Guangyu Wang, Haoyang Liu, Guiguan Yang

|Dec 09, 2024
Intron retention caused by a canonical splicing variant in SSR4-related congenital disorder of glycosylation.

Quanquan Wang, Guangyu Wang, Bing Liang

|Nov 15, 2024
Expanding the spectrum of HSPB8-related myopathy: a novel mutation causing atypical pediatric-onset axial and limb-girdle involvement with autophagy abnormalities and molecular dynamics studies.

Guiguan Yang, Xiaoqing Lv, Mengqi Yang

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Frequent Collaborators

7 joint publications

Chuanzhu Yan

1 joint publications

Guangyu Wang

1 joint publications

Haoyang Liu

1 joint publications

Guiguan Yang