Paul van Bilsen,Eric N. Burright,William F. Kaemmerer,Leonie Jaspers,Maria Stella Lombardi
申请号：
US12601292
公开号：
US20120172409A1
申请日:
2008.05.22
申请国别(地区):
US
年份:
2012
代理人:
摘要：
Methods and kits are provided for determining which single nucleotide polymorphism (“SNP”) variant of an allele of a heterozygous patient is on the same allele as a disease-causing mutation. Also, provided are kits for multi-SNP diagnosis and treatment, targeting combinations of SNPs having greater joint prevalence of heterozygosity in Huntingtons population than individual SNPs considered individually.
