<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Glycine encephalopathy Archives - Laboratory Notes</title>
	<atom:link href="https://www.laboratorynotes.com/tag/glycine-encephalopathy/feed/" rel="self" type="application/rss+xml" />
	<link>https://www.laboratorynotes.com/tag/glycine-encephalopathy/</link>
	<description></description>
	<lastBuildDate>Sat, 19 Sep 2026 22:22:29 +0000</lastBuildDate>
	<language>en</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1</generator>
	<item>
		<title>Glycine and Nonketotic Hyperglycinemia</title>
		<link>https://www.laboratorynotes.com/glycine-and-nonketotic-hyperglycinemia/</link>
					<comments>https://www.laboratorynotes.com/glycine-and-nonketotic-hyperglycinemia/#respond</comments>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Sat, 19 Sep 2026 22:22:29 +0000</pubDate>
				<category><![CDATA[Lab Notes]]></category>
		<category><![CDATA[Lab Notes: Biochemistry]]></category>
		<category><![CDATA[Lab Notes: Molecular Biology]]></category>
		<category><![CDATA[Amino acids]]></category>
		<category><![CDATA[Folate Metabolism]]></category>
		<category><![CDATA[Genetic disorders]]></category>
		<category><![CDATA[Glycine]]></category>
		<category><![CDATA[Glycine encephalopathy]]></category>
		<category><![CDATA[Metabolic disorders]]></category>
		<category><![CDATA[Metabolism]]></category>
		<category><![CDATA[Neurotransmission]]></category>
		<category><![CDATA[Nonketotic hyperglycinemia]]></category>
		<category><![CDATA[Protein]]></category>
		<guid isPermaLink="false">https://www.laboratorynotes.com/?p=31578</guid>

					<description><![CDATA[<p>Nonketotic hyperglycinemia is an inherited metabolic disorder associated with impaired glycine breakdown and accumulation of glycine, particularly in the central nervous system. Explore the glycine cleavage system, GLDC, AMT, GCSH, DLD, glycine metabolism, neurological effects, diagnosis, genetics, and related metabolic pathways.</p>
<p>The post <a href="https://www.laboratorynotes.com/glycine-and-nonketotic-hyperglycinemia/">Glycine and Nonketotic Hyperglycinemia</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
]]></description>
		
					<wfw:commentRss>https://www.laboratorynotes.com/glycine-and-nonketotic-hyperglycinemia/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
	</channel>
</rss>
