A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington’s Disease Symptoms-Reference-Cited by-同舟云学术

A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington’s Disease Symptoms

Published:2018-04-04 Issue:3 Volume:22 Page:353-359
ISSN:1177-1062
Container-title:Molecular Diagnosis & Therapy
language:en
Short-container-title:Mol Diagn Ther

Author:

Chheda Pratiksha^ORCID,Chanekar Milind,Salunkhe Yogita,Dama Tavisha,Pais Anurita,Pande Shailesh,Bendre Rajesh,Shah Nilesh

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,Genetics,Molecular Medicine,General Medicine

Link

http://link.springer.com/article/10.1007/s40291-018-0327-y/fulltext.html

Reference26 articles.

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3. Squitieri F, Gellera C, Cannella M, Mariotti C, Cislaghi G, Rubinsztein DC, et al. Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course. Brain. 2003. https://doi.org/10.1093/brain/awg077946-955F .

4. Govert F, Schneider SA. Huntington’s disease and Huntington’s disease-like syndromes: an overview. Curr Opin Neurol. 2013;4:420–7. https://doi.org/10.1097/WCO.0b013e3283632d90 .

5. Schneide SA, Walker RH, Bhatia KP. The Huntington’s disease-like syndromes: what to consider in patients with a negative Huntington’s disease gene test. Nat Clin Pract Neurol. 2007;3:517–25. https://doi.org/10.1038/ncpneuro0606 .

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