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657del5 Mutation of the Nijmegen Breakage Syndrome Gene (NBS1) in the Turkish Population

✍ Scribed by MUSTAFA TEKIN, DUYGU AKCAYOZ, CANAN UCAR, HUSEYIN GULEN and NEJAT AKAR

Book ID: 124797304
Publisher: Wayne State University Press
Year: 2005
Tongue: English
Weight: 635 KB
Volume: 77
Category: Article
ISSN: 0018-7143
DOI: 10.2307/41466334

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## Abstract The __NBS1__ gene mutation, 657del5, frequent in the Slavic populations of Central Europe, is found in most patients with Nijmegen breakage syndrome (NBS), a recessive autosomal disorder with a very high incidence of non‐Hodgkin lymphoma (NHL). We have previously described 2 heterozygou