ELOVL5 Mutations Cause Spinocerebellar Ataxia 38-Reference-Cited by-同舟云学术

ELOVL5 Mutations Cause Spinocerebellar Ataxia 38

Published:2014-08 Issue:2 Volume:95 Page:209-217
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Di Gregorio Eleonora,Borroni Barbara,Giorgio Elisa,Lacerenza Daniela,Ferrero Marta,Lo Buono Nicola,Ragusa Neftj,Mancini Cecilia,Gaussen Marion,Calcia Alessandro,Mitro Nico,Hoxha Eriola,Mura Isabella,Coviello Domenico A.,Moon Young-Ah,Tesson Christelle,Vaula Giovanna,Couarch Philippe,Orsi Laura,Duregon Eleonora,Papotti Mauro Giulio,Deleuze Jean-François,Imbert Jean,Costanzi Chiara,Padovani Alessandro,Giunti Paola,Maillet-Vioud Marcel,Durr Alexandra,Brice Alexis,Tempia Filippo,Funaro Ada,Boccone Loredana,Caruso Donatella,Stevanin Giovanni,Brusco Alfredo

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference34 articles.

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3. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Durr;Lancet Neurol.,2010

4. Cerebellar disorders—at the crossroad of molecular pathways and diagnosis;Manto;Cerebellum,2009

5. Movement disorders in spinocerebellar ataxias;van Gaalen;Mov. Disord.,2011

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