The Jews of Kurdistan are a small inbred population with a high incide
nce of beta-thalassaemia and glucose-6-phosphate dehydrogenase (G6PD)
deficiency. Recently, it was reported that the beta-thalassaemia in th
is population shows an unusual mutational diversity; 13 different muta
tions were identified, of which 4 had not previously been observed in
any other population. In contrast, we now report that the G6PD deficie
ncy, which has the highest known incidence in the world, and which aff
ects about 70% of males, is almost entirely attributable to a single w
idespread mutation, G6PD Mediterranean.