Rare gene diseases

In born genetic neurological diseases are rare and caused by a single gene mutations. There are more than 2000 genes that are involved in Mendelian heritable diseases. Early diagnosis of these single gene mutations during pregnancy or in newborns will improve treatment conditions before severe symptoms appear. NeuroQR provides multiplex TaqMan and semiconductor sequencing primer sets for testing rare genetic neurological diseases.


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Dept. of Biology
300 Pompton Road
William Paterson University
Wayne, NJ 07470

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