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RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance ( SDHD c.314+3A>T) in Splicing Site Consensus Sequences.

Hyunjung GuJinyoung HongWoochang LeeSung-Bae KimSail ChunWon-Ki Min
Published in: Annals of laboratory medicine (2022)
Keyphrases
  • single cell
  • clinical practice
  • genetic diversity