ObjectiveIn Caucasian population, the most common molecular basis for C8β deficiency is a single C→T transition in exon 9 of C8β gene resulting in a stop codon.

Cloning and Sequencing of Recombinant cDNA Encoding Human Protein Kinase CK2 β Subunit;

Cloning and analysis of beta subunit sequence of phycoerythrin gene from Corallina officinalis;

Nucleotide sequence of cloned cDNA for β-subunit of goat follicle stimulating hormone and its sequence analysis;