A novel nonsense mutation found in the CD177 gene of Thai individuals with the HNA-2 null phenotype.

Kanokpol SiriphanthongSawang PetvisesJeeraphong ThanongsaksrikulKamphon IntharanutOytip Nathalang

Published in: Transfusion medicine (Oxford, England) (2019)

The c.787A>T is a primary genetic hallmark to determine the HNA-2 null phenotype. Additional screening of the novel c.1254G>A in combination with c.787A>T is a suitable, convenient and effective diagnosis among Thais.

Keyphrases

genome wide
copy number
dna methylation
gene expression
transcription factor