Literature DB >> 26739247

RAB39B mutations are a rare finding in Parkinson disease patients.

Tobias Löchte1, Norbert Brüggemann2, Eva-Juliane Vollstedt3, Patricia Krause4, Aloysius Domingo5, Raymond Rosales6, Lillian V Lee7, Franziska Hopfner8, Ana Westenberger1, Andrea Kühn4, Christine Klein1, Katja Lohmann9.   

Abstract

Entities:  

Keywords:  Parkinson disease; RAB39B; Variant; X-linked

Mesh：

Substances：

Year:  2015        PMID： 26739247     DOI： 10.1016/j.parkreldis.2015.12.014

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN： 1353-8020            Impact factor:   4.891


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  2 in total

1.  RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies.

Authors:  Kyndall Hodges; Sheridan S Brewer; Catherine Labbé; Alexandra I Soto-Ortolaza; Ronald L Walton; Audrey J Strongosky; Ryan J Uitti; Jay A van Gerpen; Nilüfer Ertekin-Taner; Kejal Kantarci; Val J Lowe; Joseph E Parisi; Rodolfo Savica; Jonathan Graff-Radford; David T Jones; David S Knopman; Ronald C Petersen; Melissa E Murray; Neill R Graff-Radford; Tanis J Ferman; Dennis W Dickson; Zbigniew K Wszolek; Bradley F Boeve; Owen A Ross; Oswaldo Lorenzo-Betancor
Journal:  Neurobiol Aging       Date:  2016-03-24       Impact factor: 4.673

Review 2.  The Role of Rab Proteins in Parkinson's Disease Synaptopathy.

Authors:  Arianna Bellucci; Francesca Longhena; Maria Grazia Spillantini
Journal:  Biomedicines       Date:  2022-08-10
  2 in total

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