A novel homozygous TPM1 mutation in familial pediatric hypertrophic cardiomyopathy and in silico screening of potential targeting drugs.

No abstract is available for this paper.

• Publication year

  2020

• Venue

  European Review for Medical and Pharmacological Sciences

• Publication date

  2020-07-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.26355/eurrev_202007_22299PMID 32744700
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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