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657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.

Mustafa Tekin, Duygu Akcayoz, Canan Ucar, Huseyin Gulen, Nejat Akar
Human Biology 2005 June
The 657del5 mutation of the NBS1 gene has been demonstrated in most patients with Nijmegen breakage syndrome (NBS). We identified four Turkish families in which probands were diagnosed as having NBS and found to be homozygous for the 657del5 mutation. The 657del5 allele in the four Turkish families had a single origin.

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