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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ahmadpour-Yazdi, Hossein, Hormozi-Nezhad, Mohammad, Abadi, Ali, Sanati, Mohammad Hossein, Kazemi, Bahram
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Tabriz University of Medical Sciences 2013
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3892738/
https://ncbi.nlm.nih.gov/pubmed/24455482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5681/bi.2013.037
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg