Functional Validation of a Novel Homozygous TTN Splice‐Site Variant Reveals Aberrant Splicing in Hypertrophic Cardiomyopathy
PMID: 42698999
Gene: TNN
HGNC ID:11949
Functional Validation of a Novel Homozygous TTN Splice‐Site Variant Reveals Aberrant Splicing in Hypertrophic Cardiomyopathy
PMID: 42698999
Gene: TNN
HGNC ID:11949