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A novel cisAB allele with a missense variant (c.971T>C) in the ABO gene of a Brazilian family.

Marcos Paulo MiolaCaroline Luise ProchaskaGuilherme CardosoOctávio Ricci JuniorLuiz Carlos de Mattos
Published in: Vox sanguinis (2024)
phenotype.
Keyphrases
  • intellectual disability
  • copy number
  • genome wide
  • genome wide identification
  • autism spectrum disorder