Data di Pubblicazione:
2024
Abstract:
: Sequencing of DNA is normally the final procedure carried out to determine the actual pathogenic variants when the techniques used for genotyping are unable to provide complete identification of both AAT alleles. Gene sequencing of complete SERPINA1 gene by using the Sanger method or next-generation sequencing (NGS) is crucial to enable correct diagnosis in patients with alpha1-antitrypsin deficiency caused by uncommon AAT variants.This protocol explains how to correctly sequence SERPINA1 gene both with Sanger method and NGS.
Tipologia CRIS:
2.1 Contributo in volume (Capitolo o Saggio)
Keywords:
Intron sequencing; Next-generation sequencing; Rare mutations; SERPINA1
Elenco autori:
Barzon, V.; Ferrarotti, I.; Ottaviani, S.
Link alla scheda completa:
Titolo del libro:
Alpha1-antitrypsin
Pubblicato in: