First insights into the genetics of 21-hydroxylase deficiency in the Roma population.
Mirjana KocovaVioleta AnastasovskaAleksandar PetlichkovskiHenrik FalhammarPublished in: Clinical endocrinology (2021)
The Roma population in North Macedonia had a very high incidence of classic 21OHD. Almost all patients had the severe salt-wasting form and the In2G/In2G genotype.