Neurofibromatosis Type 1 Molecular and Cellular Biology /

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...

Full description

Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Upadhyaya, Meena (Editor), Cooper, David N. (Editor)
Format: Electronic eBook
Language:English
Published: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2012.
Subjects:
Medicine.
Cancer research.
Human genetics.
Molecular biology.
Neurosciences.
Oncology.
Biomedicine.
Human Genetics.
Cancer Research.
Molecular Medicine.
Online Access:Full Text via HEAL-Link

Internet

Full Text via HEAL-Link

ΒΚΠ - Πατρα: ALFd

Holdings details from ΒΚΠ - Πατρα: ALFd
Call Number: 330.01 BAU
Copy 1 Available

ΒΚΠ - Πατρα: BSC

Holdings details from ΒΚΠ - Πατρα: BSC
Call Number: 330.01 BAU
Copy 2 Available
Copy 3 Available

Similar Items