A novel role for the «Ostm1» Osteopetrotic gene in neuronal homeostasis

Osteopetrosis is a genetic disease characterized by an excess of bone resulting from a defect in the bone resorbing osteoclasts. The discovery by our lab of the Osteopetrosis associated transmembrane protein 1 (Ostm1) gene responsible for the most severe recessive osteopetrosis in both grey-lethal (...

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Bibliographic Details
Main Author: Griffiths, Adam
Other Authors: Jean Vacher (Supervisor)
Format: Others
Language:en
Published: McGill University 2010
Subjects:
Online Access:http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=86580