Literature DB >> 11094129

Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia.

P Hedera1, S DiMauro, E Bonilla, J J Wald, J K Fink.   

Abstract

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Year:  2000        PMID： 11094129     DOI： 10.1212/wnl.55.10.1591

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  2 in total

1.  Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms.

Authors:  Carl Julien; Alexandra Lissouba; Surya Madabattula; Yasmin Fardghassemi; Cory Rosenfelt; Alaura Androschuk; Joel Strautman; Clement Wong; Andrew Bysice; Julia O'sullivan; Guy A Rouleau; Pierre Drapeau; J Alex Parker; François V Bolduc
Journal:  Hum Mol Genet       Date:  2016-01-06       Impact factor: 6.150

2.  NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).

Authors:  Shirley Rainier; Jing-Hua Chai; Debra Tokarz; Robert D Nicholls; John K Fink
Journal:  Am J Hum Genet       Date:  2003-09-23       Impact factor: 11.025
  2 in total

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