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The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP
by
Umano, A.
,
Fang, K.
,
Qu, Z.
,
Scaglione, J.B.
,
Altinok, S.
,
Treadway, C.J.
,
Wick, E.T.
,
Paulakonis, E.
,
Karunanayake, C.
,
Chou, S.
,
Bardakjian, T.M.
,
Gonzalez-Alegre, P.
,
Page, R.C.
,
Schisler, J.C.
,
Brown, N.G.
,
Yan, D.
,
Scaglione, K.M.
Published in
The Journal of biological chemistry
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The Journal Of Biological Chemistry
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Subjects
Ataxia
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Biochemistry & Molecular Biology
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Chaperone
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E3 Ubiquitin Ligase
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Humans
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Life Sciences & Biomedicine
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Mutation
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Neurodegeneration
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Neurodegenerative Disease
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Science & Technology
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Spinocerebellar Ataxias - Genetics
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Spinocerebellar Ataxias - Metabolism
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Ubiquitin - Genetics
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Ubiquitin - Metabolism
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Ubiquitin-Protein Ligases - Genetics
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Ubiquitination
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