## 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
✦ LIBER ✦
Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene
✍ Scribed by Iwona Ziólkowska; Maria Mosor; Malgorzata Wierzbicka; Malgorzata Rydzanicz; Monika Pernak-Schwarz; Jerzy Nowak
- Book ID
- 108583998
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 102 KB
- Volume
- 98
- Category
- Article
- ISSN
- 1347-9032
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