Postnatal and adult consequences of loss of huntingtin during development: Implications for Huntington's disease-Reference-Cited by-同舟云学术

Postnatal and adult consequences of loss of huntingtin during development: Implications for Huntington's disease

Published:2016-12 Issue: Volume:96 Page:144-155
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Arteaga-Bracho Eduardo E.,Gulinello Maria,Winchester Michael L.,Pichamoorthy Nandini,Petronglo Jenna R.,Zambrano Alicia D.,Inocencio Julio^ORCID,De Jesus Chirstopher D.,Louie Joseph O.,Gokhan Solen,Mehler Mark F.,Molero Aldrin E.

Funder

US National Institutes of Health

F. M. Kirby, Alpern Family, Harold and Isabel Feld and Roslyn and Leslie Goldstein Foundations

Publisher

Elsevier BV

Subject

Neurology

Reference89 articles.

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3. The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin;Auerbach;Hum. Mol. Genet.,2001

4. Regional atrophy associated with cognitive and motor function in prodromal Huntington disease;Aylward;J Huntingtons Dis.,2013

5. Myelin breakdown and iron changes in Huntington's disease: pathogenesis and treatment implications;Bartzokis;Neurochem. Res.,2007

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