Colorimetric Assay for Exon 7 SMN1/SMN2 Single Nucleotide Polymorphism Using Gold Nanoprobes

Introduction: Proximal spinal muscular atrophy (SMA) is one of the most significant neurodegenerative diseases amongst the autosomal-recessive genetic disorders which is caused by the absence of protein survival of motor neuron (SMN). A critical nucleotide difference in SMN2 compared to SMN1 gene le...

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Bibliografiske detaljer

Principais autores:	Hossein Ahmadpour-Yazdi, Mohammad Reza Hormozi-Nezhad, Ali Reza Abadi, Mohammad Hossein Sanati, Bahram Kazemi
Format:	Artigo
Sprog:	Inglês
Udgivet:	Tabriz University of Medical Sciences 2013-12-01
Serier:	BioImpacts
Fag:	Colorimetric Gold Nanoprobe Nucleotide Polymorphism (SNP) Spinal Muscular Atrophy (SMA) Survival of Motor Neuron (SMN)
Online adgang:	http://journals.tbzmed.ac.ir/BI/PDF/BI-3-185.pdf
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