Phenotypic features of Huntington's disease-like 2-Reference-Cited by-同舟云学术

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Phenotypic features of Huntington's disease-like 2

Published:2003-12 Issue:12 Volume:18 Page:1527-1530
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Walker Ruth H.,Jankovic Joseph,O'Hearn Elizabeth,Margolis Russell L.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference15 articles.

1. A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion

2. A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease–like 2

3. Autosomal dominant chorea-acanthocytosis with polyglutamine-containing neuronal inclusions

4. Motor Discoordination in Mutant Mice Lacking Junctophilin Type 3

5. Familial tic disorder, parkinsonism, motor neuron disease, and acanthocytosis: A new syndrome

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1. Recent advances in non-Huntington's disease choreas;Parkinsonism & Related Disorders;2024-05

2. Chorea;Movement Disorders Phenomenology;2024

3. Huntington disease-like 2: insight into neurodegeneration from an African disease;Nature Reviews Neurology;2023-12-19

4. Chorea, Ballism, and Athetosis;Principles and Practice of Movement Disorders;2021

5. Movement Disorders and Hematologic Diseases;Movement Disorders Clinical Practice;2020-12-29

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