Literature DB >> 17659643

Codon 101 of PRKCG, a preferential mutation site in SCA14.

Dagmar Nolte, Stephan Klebe, Ralf Baron, Günther Deuschl, Ulrich Müller.   

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Year:  2007        PMID： 17659643     DOI： 10.1002/mds.21654

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  1 in total

1.  A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.

Authors:  Katherine E Hekman; Guo-Yun Yu; Christopher D Brown; Haipeng Zhu; Xiaofei Du; Kristina Gervin; Dag Erik Undlien; April Peterson; Giovanni Stevanin; H Brent Clark; Stefan M Pulst; Thomas D Bird; Kevin P White; Christopher M Gomez
Journal:  Hum Mol Genet       Date:  2012-09-21       Impact factor: 6.150
  1 in total

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