Molecular cloning of the cDNA coding for Xenopus laevis prion protein

No abstract is available for this paper.

• Publication year

  2001

• Venue

  FEBS Letters

• Publication date

  2001-11-16

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/S0014-5793(01)03027-7PMID 11718710
• 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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• SeqHelp: a program to analyze molecular sequences utilizing common computational resources.

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