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Nijmegen breakage syndrome
BACKGROUND—Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder. NBS-1, the gene defective in NBS, is located on chromosome 8q21 and has recently been cloned. The gene product, nibrin, is a novel protein, which is member of the hMre11/hRad50 protein complex, suggesting that the ge...
Gorde:
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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BMJ Group
2000
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| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1718318/ https://ncbi.nlm.nih.gov/pubmed/10799436 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/adc.82.5.400 |
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