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

[1] Margolis RL(2003)Diagnosis of Huntington disease Clin Chem 49 1726-1732

[2] Ross CA(2014)Trinucleotide repeats and haplotypes at the huntingtin locus in an Indian sample overlaps with European haplogroup a PLoS Curr 4 420-427

[3] Moily NS(2003)Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course Brain 3 517-525

[4] Kota LN(2013)Huntington’s disease and Huntington’s disease-like syndromes: an overview Curr Opin Neurol. 16 e2-985

[5] Anjanappa RM(2007)The Huntington’s disease-like syndromes: what to consider in patients with a negative Huntington’s disease gene test Nat Clin Pract Neurol 58 977-209

[6] Venugopal S(2014)American College of Medical Genetics and Genomics Standards and Guidelines for Clinical Genetics Laboratories, 2014 edition: technical standards and guidelines for Huntington disease Genet Med 18 202-595

[7] Vaidyanathan R(2000)Huntington disease: DNA analysis in Brazilian population Arq Neuropsiquiatr 25 589-65

[8] Pal P(2002)Lessons from animal models of Huntington’s disease Trends Genet 6 61-97

[9] Squitieri F(1988)Anticipation in Huntington’s disease is inherited through the male line but may originate in the female J Med Genet 10 85-351

[10] Gellera C(2004)Technical standards and guidelines for Huntington disease testing Genet Med 16 348-154

[1] Margolis RL(2003)Diagnosis of Huntington disease Clin Chem 49 1726-1732

[2] Ross CA(2014)Trinucleotide repeats and haplotypes at the huntingtin locus in an Indian sample overlaps with European haplogroup a PLoS Curr 4 420-427

[3] Moily NS(2003)Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course Brain 3 517-525

[4] Kota LN(2013)Huntington’s disease and Huntington’s disease-like syndromes: an overview Curr Opin Neurol. 16 e2-985

[5] Anjanappa RM(2007)The Huntington’s disease-like syndromes: what to consider in patients with a negative Huntington’s disease gene test Nat Clin Pract Neurol 58 977-209

[6] Venugopal S(2014)American College of Medical Genetics and Genomics Standards and Guidelines for Clinical Genetics Laboratories, 2014 edition: technical standards and guidelines for Huntington disease Genet Med 18 202-595

[7] Vaidyanathan R(2000)Huntington disease: DNA analysis in Brazilian population Arq Neuropsiquiatr 25 589-65

[8] Pal P(2002)Lessons from animal models of Huntington’s disease Trends Genet 6 61-97

[9] Squitieri F(1988)Anticipation in Huntington’s disease is inherited through the male line but may originate in the female J Med Genet 10 85-351

[10] Gellera C(2004)Technical standards and guidelines for Huntington disease testing Genet Med 16 348-154