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NBN gene mutation; nibrin gene mutation
Pathology:
- defects in the nibrin gene are associated with
a) Nijmegen breakage syndrome
b) genetic susceptibility to breast cancer
c) aplastic anemia
d) childhood acute lymphoblastic leukemia (putative)
* see nibrin
Related
nibrin; Nijmegen breakage syndrome protein 1; cell cycle regulatory protein p95 (NBN, NBS, NBS1, P95)
General
gene mutation testing; gene mutation analysis
References
Loinc