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...
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| Údar Corparáideach: | |
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| Údair Eile: | , |
| Formáid: | Leictreonach ríomhLeabhar |
| Teanga: | English |
| Foilsithe: |
Berlin, Heidelberg :
Springer Berlin Heidelberg : Imprint: Springer,
2012.
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| Eagrán: | 1st ed. 2012. |
| Ábhair: | |
| Rochtain Ar Líne: | https://doi.org/10.1007/978-3-642-32864-0 |
| Clibeanna: |
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