Neurofibromatosis Type 1 Molecular and Cellular Biology /
Neurofibromatosis type 1 (NF1), caused by mutational inactivation of the NF1 tumour suppressor gene, is one of the most common dominantly inherited human disorders, affecting 1 in 3000 individuals worldwide. This book presents in concise fashion, but as comprehensively as possible, our current state...
Saved in:
| Corporate Author: | |
|---|---|
| Other Authors: | , |
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Berlin, Heidelberg :
Springer Berlin Heidelberg : Imprint: Springer,
2012.
|
| Edition: | 1st ed. 2012. |
| Subjects: | |
| Online Access: | https://doi.org/10.1007/978-3-642-32864-0 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|