Associated Papers
LAMP2 variants in four Chinese children with Danon disease: clinical and molecular analysis in a monocentric cohort.
Lu J et al.
Cardiology in the Young, 2025
Clinical and Genetic Profile of Chinese Children With Danon Disease: A Single-Center Retrospective Cohort Study.
Zhang Q et al.
The Canadian Journal of Cardiology, 2025
Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the Literature.
Shalata A et al.
Genes, 2023
37628591 (PubMed )
Supplement: genes-14-01539-s001.zip › genes-2456230-supplementary › Supplementary_FIGURE_and_LAMP2_MUTATIONS_EXCEL_FILES › Table_S1-HGMD_LAMP2_gene_mutations.xlsx › Missense_nonsense-44_Mutations
Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort study.
Chan W et al.
Eclinicalmedicine, 2022
35747179 (PubMed )
Supplement: mmc1.pdf
A Frequent Observation of Wolff-Parkinson-White Syndrome and Fasciculoventricular Pathways in Patients With Danon Disease.
Chen X et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2022
Generation of induced pluripotent stem cells (NJDTHi001-A) from a Danon disease child with mutation of c.467 T > G in LAMP2 gene.
Zhu X et al.
Stem Cell Research, 2020
Case Report: Identification of Mutations in LAMP2 in Two Chinese Infants With Danon Disease.
Zhang L et al.
Frontiers in Genetics, 2020
Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing.
Fu L et al.
The American Journal of Cardiology, 2016
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children.
Yang Z et al.
Circulation, 2005
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