Clinical manifestations of homozygote allele carriers in Huntington disease-Reference-Cited by-同舟云学术

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Clinical manifestations of homozygote allele carriers in Huntington disease

Published:2019-03-13 Issue: Volume: Page:10.1212/WNL.0000000000007147
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Cubo Esther,Martinez-Horta Saul-Indra,Santalo Frederic Sampedro,Descalls Asunción Martínez,Calvo Sara,Gil-Polo Cecilia,Muñoz Ignacio,Llano Katia,Mariscal Natividad,Diaz Dolores,Gutierrez Aranzazu,Aguado Laura,Ramos-Arroyo María A.,

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutant huntingtin impairs neurodevelopment in human brain organoids through CHCHD2-mediated neurometabolic failure;Nature Communications;2024-08-22

2. Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease reveal shared and tissue-specific effects;2024-06-18

3. Deep behavioural phenotyping of the Q175 Huntington disease mouse model: effects of age, sex, and weight;BMC Biology;2024-05-23

4. Huntingtin loss-of-function contributes to transcriptional deregulation in Huntington’s disease;2024-05-20

5. Long somatic DNA-repeat expansion drives neurodegeneration in Huntington disease;2024-05-20

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