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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Bibliographic Details
Call Number:Libro Electrónico
Corporate Author: SpringerLink (Online service)
Other Authors: Upadhyaya, Meena (Editor), Cooper, David N. (Editor)
Format: Electronic eBook
Language:Inglés
Published: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2012.
Edition:1st ed. 2012.
Subjects:
Medical genetics.
Cancer.
Oncology.
Medicine-Research.
Biology-Research.
Neurosciences.
Medical Genetics.
Cancer Biology.
Biomedical Research.
Neuroscience.
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