AFG3L2 mutations cause autosomal dominant ataxia SCA28 and reveal an essential role of the m-AAA AGF3L2 homocomplex in the cerebellum

Authors :: Dibella, D
Lazzaro, F
Brusco, Alfredo
Battaglia, G
Pastore, A
Finardi, A
Fracasso, V
Plumari, M
Cagnoli, Claudia
Tempia, Filippo
Brussino, Alessandro
Gellera, C
Mariotti, C
Pievani, P
Didonato, S
Langer, T
Muzi Falconi, M
Taroni, F.
Publication Year :: 2008
Publisher :: The American Society of Human Genetics, 2008.

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