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The molecular basis of spinocerebellar ataxia type 48 cause..:
Umano, A.
;
Fang, K.
;
Qu, Z.
...
Journal of Biological Chemistry. 298 (2022) 5 - p. 101899 , 2022
Link:
https://doi.org/10.1016/j.jbc.2022.101899
RT Journal T1 <Title>The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.jbc.2022.101899&Exemplar=1&LAN=DE A1 Umano, A. A1 Fang, K. A1 Qu, Z. A1 Scaglione, J.B. A1 Altinok, S. A1 Treadway, C.J. A1 Wick, E.T. A1 Paulakonis, E. A1 Karunanayake, C. A1 Chou, S. A1 Bardakjian, T.M. A1 Gonzalez-Alegre, P. A1 Page, R.C. A1 Schisler, J.C. A1 Brown, N.G. A1 Yan, D. A1 Scaglione, K.M. PB Elsevier BV YR 2022 SN 0021-9258 JF Journal of Biological Chemistry VO 298 IS 5 SP 101899 LK http://dx.doi.org/https://doi.org/10.1016/j.jbc.2022.101899 DO https://doi.org/10.1016/j.jbc.2022.101899 SF ELIB - SuUB Bremen
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