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THDF1
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Novel insights on GTPBP3-associated hypertrophic cardiomyopathy.
Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcome.
Pathogenicity Analysis of a Novel Variant in GTPBP3 Causing Mitochondrial Disease and Systematic Lit…
Mechanistic study on the nuclear modifier gene MSS1 mutation suppressing neomycin sensitivity of the…
Generation of patient-derived IPSC lines from a girl with Combined Oxidative Phosphorylation Deficie…
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