PMC · DOI:10.1007/s00392-023-02190-8·April 17, 2023
Case report: cosegregation of a TPM1 in-frame deletion (p.Lys7del) with familial non-compaction cardiomyopathy (NCCM)
Yvonne Hanel, Sven Dittmann, Klara Müller, Monica Elena Ioannou, Eric Schulze-Bahr

Abstract
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Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Diseases1
Mutations1
p.Lys7del
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Taxonomy
TopicsCardiomyopathy and Myosin Studies · Muscle Physiology and Disorders · Neurogenetic and Muscular Disorders Research
