Publications by authors named "Zezhang Lin"

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Correction: Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization.
Xiongda Liang, Jiameng Si, Hongting Xie, Yuqing Guan, Wanying Lin, Zezhang Lin

Acta Neuropathol Commun· May 2025

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Application value of long-read sequencing in full characterization of thalassemia-associated structural variations: identifying a novel large segmental duplication and literature review.
Zeyan Zhong, Ganwei Zheng, Dina Zhu, Yongqiong Liu, Zezhang Lin

Orphanet J Rare Dis· April 2025

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Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization.
Xiongda Liang, Jiameng Si, Hongting Xie, Yuqing Guan, Wanying Lin, Zezhang Lin

Acta Neuropathol Commun· March 2025

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SUPT5H mutations associated with elevation of Hb A level: Identification of two novel variants and literature review.
Zezhang Lin, Xiongda Liang, Xiaofeng Wei, Guanxia Liang, Dina Zhu

Gene· May 2024

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Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype.
Guanxia Liang, Zezhang Lin, Yang Zhang, Qianqian Zhang, Dina Zhu

Mol Genet Genomics· May 2024

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A novel gain-of-function PIP4K2A mutation elevates the expression of β-globin and aggravates the severity of α-thalassemia.
Yanxia Zhang, Hongting Xie, Guanxia Liang, Yunrong Qin, Xiaofeng Wei, Yuling Xie, Zezhang Lin, Jiaqiong Lin

Br J Haematol· September 2023

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