Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

AFG3L2 mutations cause autosomal dominant ataxia SCA28 and reveal an essential role for the mitochondrial m-AAA protease complex in the cerebellum

D. Di Bella,F. Lazzaro,A. Brusco, G. Battaglia,A. Pastore,A. Finardi,V. Fracasso,M. Plumari,C. Cagnoli,F. Tempia,A. Brussino,C. Gellera,C. Mariotti,P. Plevani,S. Di Donato, T. Langer,M. Muzi-Falconi,F. Taroni

JOURNAL OF NEUROLOGY（2009）

Cited 1|Views3
No score
Key words
dominant ataxia sca28,mutations,m-aaa
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined