Watson syndrome
Source: Wikipedia, the free encyclopedia.
Medical condition
| Watson syndrome | |
|---|---|
| Specialty | Medical genetics  |
Watson syndrome is an
neurofibromatosis type 1.[2]
See also
- Westerhof syndrome
- List of cutaneous conditions
References
- ISBN 978-1-4160-2999-1.
- PMID 1770531.
External links
| Classification | |
|---|---|
| External resources |
Deficiencies of intracellular signaling peptides and proteins | |||||||
|---|---|---|---|---|---|---|---|
| GTP-binding protein regulators |
| ||||||
| G protein |
| ||||||
| MAP kinase | |||||||
| Other kinase/phosphatase |
| ||||||
| Signal transducing adaptor proteins | |||||||
| Other | |||||||
This Genodermatoses article is a stub. You can help Wikipedia by expanding it. |