Copy Number Variation, Eicosapentaenoic Acid and Neurological Disorders. With Particular Reference to Huntington’s Disease and Associated CAG Repeats, and to Myalgic Encephalomyelitis and Viral Infection

2010 ◽  
pp. 15-20 ◽  
Author(s):  
Basant K. Puri ◽  
Mehar S. Manku
Keyword(s):  
Copy Number Variation ◽  
Eicosapentaenoic Acid ◽  
Viral Infection ◽  
Huntington's Disease ◽  
Huntington’S Disease ◽  
Neurological Disorders ◽  
Copy Number ◽  
Myalgic Encephalomyelitis ◽  
Cag Repeats ◽  
Number Variation

scholarly journals Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease

2014 ◽  
Vol 23 (12) ◽  
pp. 3129-3137 ◽  
Author(s):  
A. Vittori ◽  
C. Breda ◽  
M. Repici ◽  
M. Orth ◽  
R. A. C. Roos ◽  
...  
Keyword(s):  
Copy Number Variation ◽  
Huntington's Disease ◽  
Huntington’S Disease ◽  
Copy Number ◽  
Glucose Transporter ◽  
Age Of Onset ◽  
Transporter Gene ◽  
Number Variation

C11 Copy number variation in Huntington's disease

2010 ◽  
Vol 81 (Suppl 1) ◽  
pp. A19.2-A19
Author(s):  
A Vittori ◽  
F Giorgini ◽  
F T Outeiro ◽  
E J Hollox
Keyword(s):  
Copy Number Variation ◽  
Huntington's Disease ◽  
Huntington’S Disease ◽  
Copy Number ◽  
Number Variation

The combination of whole‐exome sequencing and copy number variation sequencing enables the diagnosis of rare neurological disorders

2019 ◽  
Vol 96 (2) ◽  
pp. 140-150 ◽  
Author(s):  
Qingguo Jiao ◽  
Haiming Sun ◽  
Haoya Zhang ◽  
Ran Wang ◽  
Suting Li ◽  
...  
Keyword(s):  
Copy Number Variation ◽  
Exome Sequencing ◽  
Whole Exome Sequencing ◽  
Neurological Disorders ◽  
Copy Number ◽  
Whole Exome ◽  
Number Variation
Sign in / Sign up

Export Citation Format

Share Document