Nalaganje...
Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.
Piebaldism is an autosomal dominant genetic disorder characterized by cogenital patches of skin and hair from which melanocytes are completely absent. A similar disorder of mouse, dominant white spotting (W), results from mutations of the c-Kit protooncogene, which encodes and receptor for mast/stem...
Shranjeno v:
| Main Authors: | , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
1991
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC52576/ https://ncbi.nlm.nih.gov/pubmed/1717985 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|