Etiology of (CAG)n triplet repeat neurodegenerative diseases such as Huntington's disease is connected to stimulation of glutamate receptors-Reference-Cited by-同舟云学术

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Etiology of (CAG)n triplet repeat neurodegenerative diseases such as Huntington's disease is connected to stimulation of glutamate receptors

Published:1997-05 Issue:5 Volume:48 Page:393-398
ISSN:0306-9877
Container-title:Medical Hypotheses
language:en
Short-container-title:Medical Hypotheses

Author:

Fischer K.M.

Publisher

Elsevier BV

Subject

General Medicine

Reference66 articles.

1. Trinucleotide repeat expansions in neurological disease;Warren;Curr Opin Neurobiol,1993

2. Molecular evidence that the myxozoan protists are metazoans;Smothers;Sci,1994

3. Trinucleotide repeat expansion in neurological disease;La Spada;Ann Neurol,1994

4. A gene for familial hemiplegic migraine maps to chromosome 19;Joutel;Nat Genet,1993

5. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11;Ranum;Nat Genet,1994

Cited by 4 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. Ion channels and neuronal excitability in polyglutamine neurodegenerative diseases;Biomolecular Concepts;2022-01-01

2. Human PDE5A gene encodes three PDE5 isoforms from two alternate promoters;International Journal of Impotence Research;2002-02

3. Brain Cannabinoid Systems as Targets for the Therapy of Neurological Disorders;Neurobiology of Disease;1998-12

4. Parkinson's disease, amyotrophic lateral sclerosis and spinal muscular atrophy are caused by an unstable (CAG)n trinucleotide repeat microsatellite;Medical Hypotheses;1997-10

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