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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Détails bibliographiques
Cote:Libro Electrónico
Collectivité auteur: SpringerLink (Online service)
Autres auteurs: Upadhyaya, Meena (Éditeur intellectuel), Cooper, David N. (Éditeur intellectuel)
Format: Électronique eBook
Langue:Inglés
Publié: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2012.
Édition:1st ed. 2012.
Sujets:
Medical genetics.
Cancer.
Oncology.
Medicine-Research.
Biology-Research.
Neurosciences.
Medical Genetics.
Cancer Biology.
Biomedical Research.
Neuroscience.
Accès en ligne:Texto Completo

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