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	<title>GRK1 | Asper Biogene</title>
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	<description>with a set of efficient DNA tests</description>
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		<title>Congenital Stationary Night Blindness</title>
		<link>https://www.asperbio.com/asper-ophthalmics/congenital-stationary-night-blindness-genetic-testing-ngs-panel?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=congenital-stationary-night-blindness-csnb</link>
		
		<dc:creator><![CDATA[Marge]]></dc:creator>
		<pubDate>Thu, 22 Apr 2010 10:45:53 +0000</pubDate>
				<category><![CDATA[Määratlemata]]></category>
		<category><![CDATA[CABP4]]></category>
		<category><![CDATA[CACNA1F]]></category>
		<category><![CDATA[CACNA2D]]></category>
		<category><![CDATA[Congenital Stationary Night Blindness]]></category>
		<category><![CDATA[CSNB]]></category>
		<category><![CDATA[GNAT1]]></category>
		<category><![CDATA[GRK1]]></category>
		<category><![CDATA[GRM6]]></category>
		<category><![CDATA[NYX]]></category>
		<category><![CDATA[PDE6B]]></category>
		<category><![CDATA[RHO]]></category>
		<category><![CDATA[SAG]]></category>
		<category><![CDATA[TRPM1]]></category>
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					<description><![CDATA[<p>Congenital Stationary Night Blindness NGS panel Genes (full coding region): CABP4, CACNA1F, CHM, GNAT1, GRK1, GRM6, NYX, PDE6B, RDH5, RHO, SAG, SLC24A1, TRPM1 List of diseases covered by the panel Lab method: TAT: 6-9 weeks Specimen requirements: 2-4 ml of blood with anticoagulant EDTA 1 µg DNA in TE, AE or pure sterile water at [&#8230;]</p>
The post <a href="https://www.asperbio.com/asper-ophthalmics/congenital-stationary-night-blindness-genetic-testing-ngs-panel">Congenital Stationary Night Blindness</a> first appeared on <a href="https://www.asperbio.com">Asper Biogene - genetic testing company</a>.]]></description>
		
		
		
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