Characterisation of non-coding genetic variation in histamine receptors using AnNCR-SNP

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Amino Acids

• Publication date

  2016-06-06

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00726-016-2265-5PMID 27270572
• 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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  2015influential reference
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  2002cited by this paper
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  2000cited by this paper

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