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2. Comprehensive review on gene mutations contributing to dilated cardiomyopathy
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3. LRRC10 (Leucine‐Rich Repeat Containing Protein 10) and REEP5 (Receptor Accessory Protein 5) as Novel Regulators of Cardiac Excitation‐Contraction Coupling Structure and Function
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4. CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy
   Xing-Biao Qiu et al, 2017, Clinical Chemistry and Laboratory Medicine (CCLM) CrossRef
5. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system
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6. The Role of Leucine-Rich Repeat Containing Protein 10 (LRRC10) in Dilated Cardiomyopathy
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7. Multi-omics assessment of dilated cardiomyopathy using non-negative matrix factorization
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8. Unraveling the mechanisms of cardiomyocyte proliferation and maturation in regenerative cardiac medicine
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10. Epigenomic and Transcriptomic Dynamics During Human Heart Organogenesis
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11. Pediatric Dilated Cardiomyopathy‐Associated LRRC10 (Leucine‐Rich Repeat–Containing 10) Variant Reveals LRRC10 as an Auxiliary Subunit of Cardiac L‐Type Ca 2+ Channels
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12. Molecular pathological study on LRRC10 in sudden unexplained nocturnal death syndrome in the Chinese Han population
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13. Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies
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14. LRRC10 is required to maintain cardiac function in response to pressure overload
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15. Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review
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16. Leucine Rich Repeat Proteins: Sequences, Mutations, Structures and Diseases
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17. VCAM1 expression in the myocardium is associated with the risk of heart failure and immune cell infiltration in myocardium
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18. Heart Regeneration in the Mexican Cavefish
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19. Understanding the molecular basis of cardiomyopathy
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