Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy

Publisher:

New England Journal of Medicine

Date published:

2013

Record type:

Journal article

Corporate Author:

The Multiple-System Atrophy Research Collaboration

Journal Title:

The New England Journal of Medicine

Source:

The New England Journal of Medicine, Vol. 369, No. 3, July 18, 2013, pp. 233-244

Subject:

MULTIPLE-SYSTEM ATROPHY

NEURODEGENERATIVE DISEASE

Abstract:

Multiple-system atrophy is a rare neurodegenerative disease characterized by autonomic failure. Mutations affecting an enzyme essential for the synthesis of coenzyme Q10 confer susceptibility to the disease in some persons.

Language:

English

Catagory URL:

http://www.nejm.org

CITATION: The Multiple-System Atrophy Research Collaboration. Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy . : New England Journal of Medicine , 2013. The New England Journal of Medicine, Vol. 369, No. 3, July 18, 2013, pp. 233-244 - Available at: https://library.au.int/mutations-coq2-familial-and-sporadic-multiple-system-atrophy-4