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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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Bibliografske podrobnosti
Korporativna značnica: SpringerLink (Online service)
Drugi avtorji: Upadhyaya, Meena. (Editor, http://id.loc.gov/vocabulary/relators/edt), Cooper, David N. (Editor, http://id.loc.gov/vocabulary/relators/edt)
Format: Elektronski eKnjiga
Jezik:English
Izdano: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2012.
Izdaja:1st ed. 2012.
Teme:
Human genetics.
Cancer research.
Oncology  .
Molecular biology.
Neurosciences.
Human Genetics.
Cancer Research.
Oncology.
Molecular Medicine.
Online dostop:https://doi.org/10.1007/978-3-642-32864-0
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