Literature DB >> 17582354

Heterozygous mutations in genes causing parkinsonism: monogenic disorders go complex.

Enza Maria Valente, Alessandro Ferraris.   

Abstract

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Mesh：

Year:  2007        PMID： 17582354     DOI： 10.1016/S1474-4422(07)70158-8

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN： 1474-4422            Impact factor:   44.182


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  3 in total

Review 1.  DJ-1, PINK1, and their effects on mitochondrial pathways.

Authors:  Mark R Cookson
Journal:  Mov Disord       Date:  2010       Impact factor: 10.338

2.  Subclinical sensory abnormalities in unaffected PINK1 heterozygotes.

Authors:  Mirta Fiorio; Enza Maria Valente; Mattia Gambarin; Anna Rita Bentivoglio; Tamara Ialongo; Alberto Albanese; Paolo Barone; Maria Teresa Pellecchia; Francesco Brancati; Giuseppe Moretto; Antonio Fiaschi; Michele Tinazzi
Journal:  J Neurol       Date:  2008-07-03       Impact factor: 4.849

3.  Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus.

Authors:  Jonas Carlsson Almlöf; Sara Nystedt; Dag Leonard; Maija-Leena Eloranta; Giorgia Grosso; Christopher Sjöwall; Anders A Bengtsson; Andreas Jönsen; Iva Gunnarsson; Elisabet Svenungsson; Lars Rönnblom; Johanna K Sandling; Ann-Christine Syvänen
Journal:  Hum Genet       Date:  2019-02-01       Impact factor: 4.132
  3 in total

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