Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency.
- Resource Type
- Article
- Source
- Familial Cancer; Oct2016, Vol. 15 Issue 4, p587-591, 5p
- Subject
- Language
- ISSN
- 13899600