NBN gene mutation; nibrin gene mutation
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Contents
1
Pathology
2
More general terms
3
Additional terms
4
References
Pathology
defects in the
nibrin
gene are associated with
Nijmegen breakage syndrome
genetic susceptibility to breast cancer
aplastic anemia
childhood
acute lymphoblastic leukemia
(
putative
)
* see
nibrin
More general terms
gene mutation testing; gene mutation analysis
Additional terms
nibrin; Nijmegen breakage syndrome protein 1; cell cycle regulatory protein p95 (NBN, NBS, NBS1, P95)
References
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