Literature DB >> 25863969

Erratum to: The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together.

A Duarri1, E Nibbeling, M R Fokkens, M Meijer, E Boddeke, E Lagrange, G Stevanin, A Brice, A Durr, D S Verbeek.   

Abstract

Entities:  

Year:  2015        PMID： 25863969     DOI： 10.1007/s10048-015-0447-z

Source DB:  PubMed          Journal:  Neurogenetics        ISSN： 1364-6745            Impact factor:   2.660


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  3 in total

1.  Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19.

Authors:  Martin Paucar; Åsa Bergendal; Peter Gustavsson; Magnus Nordenskjöld; José Laffita-Mesa; Irina Savitcheva; Per Svenningsson
Journal:  Cerebellum       Date:  2018-08       Impact factor: 3.847

2.  Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22.

Authors:  Mengjie Li; Fen Liu; Xiaoyan Hao; Yu Fan; Jiadi Li; Zhengwei Hu; Jingjing Shi; Liyuan Fan; Shuo Zhang; Dongrui Ma; Mengnan Guo; Yuming Xu; Changhe Shi
Journal:  Front Mol Neurosci       Date:  2022-06-23       Impact factor: 6.261

3.  Molecular basis of degenerative spinal disorders from a proteomic perspective (Review).

Authors:  Chang Liu; Minghui Yang; Libangxi Liu; Yang Zhang; Qi Zhu; Cong Huang; Hongwei Wang; Yaqing Zhang; Haiyin Li; Changqing Li; Bo Huang; Chencheng Feng; Yue Zhou
Journal:  Mol Med Rep       Date:  2019-11-12       Impact factor: 2.952
  3 in total

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