Nalaganje...
Melanoma cases demonstrate increased carrier frequency of Phenylketonuria/hyperphenylalanemia mutations
Identifying novel melanoma genetic risk factors informs screening and prevention efforts. Mutations in the phenylalanine hydroxylase gene (the causative gene in phenylketonuria) lead to reduced pigmentation in untreated phenylketonuria patients, and reduced pigmentation is associated with greater me...
Shranjeno v:
| izdano v: | Pigment Cell Melanoma Res |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2018
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6013363/ https://ncbi.nlm.nih.gov/pubmed/29473999 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pcmr.12695 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|