Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in <i>MYO15A</i> as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

<div class="floats-full-page floats-full-page-figure"><h2>Figure 3</h2><div class="floats-full-page-caption"><div>Sanger sequencing results of the c.3658_3662del and c.6177+1G&gt;T mutations in the family members.</div></div><div class="floats-full-page-content"><table class="figure-group"><tr class="fig-image" id="a"><td><object data="https://static-01.hindawi.com/articles/np/volume-2020/6350479/figures/6350479.fig.003a.svgz" name="6350479.fig.003a" type="image/svg+xml"></object></td></tr><tr class="fig-caption"><td><b>(a) </b></td></tr><tr class="fig-image" id="b"><td><object data="https://static-01.hindawi.com/articles/np/volume-2020/6350479/figures/6350479.fig.003b.svgz" name="6350479.fig.003b" type="image/svg+xml"></object></td></tr><tr class="fig-caption"><td><b>(b) </b></td></tr></table></div></div>

Figure 3 | Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in <i>MYO15A</i> as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

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Figure 3: Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in <i>MYO15A</i> as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

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Figure 3 | Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

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<p><em>Neural Plasticity</em> is an interdisciplinary journal dedicated to the publication of articles related to all aspects of neural plasticity, with special emphasis on its functional significance as reflected in behavior and in psychopathology.</p>


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<p>Chief Editor, Professor Baudry, is currently University Professor at Western University of Health Sciences in Pomona, CA. His research focuses on understanding the molecular/cellular mechanisms of learning and memory and neurodegeneration.</p>


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