Mutant Prion Protein D202N Associated with Familial Prion Disease is Retained in the Endoplasmic Reticulum and Forms ‘Curly’ Intracellular Aggregates

Author: Gu Yaping   Verghese Susamma   Bose Sharmila   Mohan Maradumane   Singh Neena  

Publisher: Humana Press, Inc

ISSN: 0895-8696

Source: Journal of Molecular Neuroscience, Vol.32, Iss.1, 2007-05, pp. : 90-96

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