Article
<i>In silico</i> analysis of coding SNPs and 3′-UTR associated miRNAs in <i>DCAF17</i> gene that may affect the regulation and pathogenesis of Woodhouse-Sakati Syndrome
2019-04-07
Abstract excerpt
<h4>Background</h4> Woodhouse-Sakati Syndrome refers to a group of inherited disorders characterized by alopecia, hypogonadism, diabetes mellitus, hypothyroidism and progressive extrapyramidal signs. The aim of this study is to identify the pathogenic SNPs in the DCAF17 gene with their related mciroRNAs and their effect on the structure and function of the protein. <h4>Material and Methods</h4> We used differe...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 1d45b9a5-438e-5af7-97d6-340c5c4a0e05
- DOI
- 10.1101/601310
