Minting Lin
Fuzhou, 350212, China
Last Updated: 09/26/2026
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Found 14 publications
Assessing the multidimensional burden of facioscapulohumeral muscular dystrophy through patient-reported outcomes and experience.
Journal: Journal of patient-reported outcomes
Published: August 09, 2025
Bi-allelic loss-of function variants in ATP2A1 cause autosomal recessive Brody disease.
Journal: QJM : monthly journal of the Association of Physicians
Published: July 07, 2025
Association of Diaphragm Involvement Assessed by Ultrasound With Disease Severity in Facioscapulohumeral Muscular Dystrophy.
Journal: Journal of cachexia, sarcopenia and muscle
Published: September 11, 2024
Age at onset mediates genetic impact on disease severity in facioscapulohumeral muscular dystrophy.
Journal: Brain : a journal of neurology
Published: April 25, 2024
CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: September 26, 2023
An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1.
Journal: Brain : a journal of neurology
Published: April 04, 2023
Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy.
Journal: Neurology
Published: November 29, 2022
Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study.
Journal: The Lancet regional health. Western Pacific
Published: January 13, 2022
Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population.
Journal: Brain : a journal of neurology
Published: January 06, 2022
Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1.
Journal: Stem cell research
Published: August 05, 2021
Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy.
Journal: Journal of medical genetics
Published: October 17, 2019
Last Updated: 09/26/2026