Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies.

No abstract is available for this paper.

• Publication year

  2014

• Venue

  Clinica chimica acta; international journal of clinical chemistry

• Publication date

  2014-06-10

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.cca.2014.03.032PMID 24721642
• 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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