Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome

No abstract is available for this paper.

• Publication year

  1998

• Venue

  Human Genetics

• Publication date

  1998-03-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s004390050690PMID 9544837
• 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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• (2020). Serine mutation of a conserved threonine in the hERG K+ channel S6-pore region leads to loss-of-function through trafficking impairment.

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