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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>Journal of Research in Medical Sciences</JournalTitle><Issn>1735-1995</Issn><Volume>22</Volume><Issue>8</Issue><PubDate PubStatus="epublish"><Year>2017</Year><Month>05</Month><Day>05</Day></PubDate></Journal><title locale="en_US">Diverse pattern of gap junction beta?2 and gap junction beta?4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran</title><FirstPage>10687</FirstPage><LastPage>10687</LastPage><Language>EN</Language><AuthorList><Author/><Author/><Author/><Author/><Author/><Author/><Author/><Author/></AuthorList><History><PubDate PubStatus="received"><Year>2017</Year><Month>07</Month><Day>22</Day></PubDate></History><abstract locale="en_US">&lt;table class="NormalTable"&gt;&lt;tbody&gt;&lt;tr&gt;&lt;td width="550"&gt;&lt;span class="fontstyle0"&gt;Background: &lt;/span&gt;&lt;span class="fontstyle2"&gt;We aimed to determine the contribution of four DFNB loci and mutation analysis of gap junction beta?2 (&lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2) &lt;/span&gt;&lt;span class="fontstyle2"&gt;and &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;genes in autosomal recessive nonsyndromic hearing loss (ARNSHL) in South of Iran. &lt;/span&gt;&lt;span class="fontstyle0"&gt;Materials and Methods: &lt;/span&gt;&lt;span class="fontstyle2"&gt;A total of 36 large ARNSHL pedigrees with at least two a?ected subjects were enrolled in the current study. Te &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;and &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;genes mutations were screened using direct sequencing method. Te &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;and &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;negative families were analyzed for the linkage to DFNB21, DFNB24, DFNB29, and DFNB42 loci by genotyping the  corresponding STR markers using polymerase chain reaction?PAGE method. &lt;/span&gt;&lt;span class="fontstyle0"&gt;Results: &lt;/span&gt;&lt;span class="fontstyle2"&gt;We found a homozygous nonsense mutation W77X and a homozygous missense mutation C169W in 5.55% of studied families in &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;and &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;genes, respectively. Five heterozygous mutations including V63G, A78T, and R127H in &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;gene, and R103C and R227W in &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;gene were detected. We identifed two novel variations V63G in &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;and R227W in &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4&lt;/span&gt;&lt;span class="fontstyle2"&gt;. &lt;/span&gt;&lt;span class="fontstyle3"&gt;In silico &lt;/span&gt;&lt;span class="fontstyle2"&gt;analysis predicted that both novel variations are deleterious mutations. We did not unveil any linkage between DFNB21, DFNB24, DFNB29, and DFNB42 loci and ARNSHL among studied families. &lt;/span&gt;&lt;span class="fontstyle0"&gt;Conclusion: &lt;/span&gt;&lt;span class="fontstyle2"&gt;Tis is the frst report of &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;and &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;mutations from Hormozgan population. According to the previous publications regarding &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB2 &lt;/span&gt;&lt;span class="fontstyle2"&gt;and &lt;/span&gt;&lt;span class="fontstyle3"&gt;GJB4 &lt;/span&gt;&lt;span class="fontstyle2"&gt;mutations, the distribution of the mutations is di?erent from other parts of Iran that should be considered in primary health?care programs. Further investigations are needed to evaluate the contribution of other loci in ARNSHL subjects in South of Iran.&lt;br /&gt;&lt;/span&gt;&lt;/td&gt;&lt;/tr&gt;&lt;/tbody&gt;&lt;/table&gt;&lt;br /&gt; &lt;br style="font-style: normal; font-variant: normal; font-weight: normal; letter-spacing: normal; line-height: normal; orphans: 2; text-align: -webkit-auto; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px;" /&gt;</abstract><web_url>http://jrms.mui.ac.ir/index.php/jrms/article/view/10687</web_url><pdf_url>http://jrms.mui.ac.ir/index.php/jrms/article/download/10687/5475</pdf_url></Article></Articles>
