| Literature DB >> 23665167 |
Aditya K Padhi1, Suhas V Vasaikar, Bhyravabhotla Jayaram, James Gomes.
Abstract
Certain single nucleotide polymorphisms causing missense mutations in angiogenin result in its loss-of-function and onset of amyotrophic lateral sclerosis (ALS). Although several such associations are reported across diverse ethnic groups, no method is available for predicting if a new mutation is deleterious. We present here a fast molecular dynamics based method for determining the mechanisms of functional loss caused by mutations, and attributes to ascertain whether a mutation causes ALS.Entities:
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Year: 2013 PMID: 23665167 DOI: 10.1016/j.febslet.2013.04.022
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124