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	<title>ATXN8 - Bion Genetic</title>
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		<title>Spinocerebellar Ataxia (SCA)</title>
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<h1 class="header-title">Spinocerebellar Ataxia (SCA)</h1>
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<a href="https://biongenetic.com/test-categories/molecular-genetics/">Molecular Genetics</a> / <a href="https://biongenetic.com/test-categories/trinucleotide-repeat-analysis/">Trinucleotide Repeat Analysis</a>


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<p>The autosomal-dominant spinocerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by slowly progressive cerebellar dysfunction. The most common types of SCAs are 1, 2, 3, 6 and 7 (caused by CAG trinucleotide repeats) and SCA8 (CTA/CTG expansions).</p>

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<p>5-7 weeks</p>

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<p>NGS</p>

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<p>EDTA Blood ,DNA</p>

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<p>6</p>

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<a href="https://biongenetic.com/genes/atxn1/">ATXN1</a>,   <a href="https://biongenetic.com/genes/atxn2/">ATXN2</a>,   <a href="https://biongenetic.com/genes/atxn3/">ATXN3</a>,   <a href="https://biongenetic.com/genes/atxn7/">ATXN7</a>,   <a href="https://biongenetic.com/genes/atxn8/">ATXN8</a>,   <a href="https://biongenetic.com/genes/cacna1a/">CACNA1A</a>

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	</section><p>The post <a href="https://biongenetic.com/tests/spinocerebellar-ataxia-sca/">Spinocerebellar Ataxia (SCA)</a> first appeared on <a href="https://biongenetic.com">Bion Genetic</a>.</p>]]></content:encoded>
					
		
		
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