The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP

por 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.
Publicado 2022