Login / Signup

A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B w phenotype.

Annika K HultÅsa HellbergJill R StorryMartin PísackaMartin L Olsson
Published in: Transfusion (2022)
Keyphrases
  • intellectual disability
  • copy number
  • genome wide
  • genome wide identification
  • gene expression
  • dna methylation
  • autism spectrum disorder