Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis-Reference-Cited by-同舟云学术

Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis

Published:2017-10 Issue: Volume:58 Page:239.e11-239.e20
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Teyssou Elisa,Chartier Laura,Amador Maria-Del-Mar,Lam Roselina,Lautrette Géraldine,Nicol Marie,Machat Selma,Da Barroca Sandra,Moigneu Carine,Mairey Mathilde,Larmonier Thierry,Saker Safaa,Dussert Christelle,Forlani Sylvie,Fontaine Bertrand,Seilhean Danielle,Bohl Delphine,Boillée Séverine,Meininger Vincent,Couratier Philippe,Salachas François,Stevanin Giovanni^ORCID,Millecamps Stéphanie

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

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