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- Q3053945 subject Q6812688.
- Q3053945 subject Q6902466.
- Q3053945 subject Q7215445.
- Q3053945 abstract "Template:ForGlycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism. The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism. There are several forms of the disease, with varying severity of symptoms and time of onset. The symptoms are exclusively neurological in nature, and clinically this disorder is characterized by abnormally high levels of the amino acid glycine in bodily fluids and tissues, especially the cerebral spinal fluid. Glycine encephalopathy is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients with the disorder, and to distinguish it from the disorders that cause "ketotic hyperglycinemia" (seen in propionic acidemia and several other inherited metabolic disorders). To avoid confusion, the term "glycine encephalopathy" is often used, as this term more accurately describes the clinical symptoms of the disorder.".
- Q3053945 thumbnail Glycin_-_Glycine.svg?width=300.
- Q3053945 wikiPageExternalLink glycine-encephalopathy.
- Q3053945 wikiPageExternalLink www.nkh-network.org.
- Q3053945 wikiPageExternalLink nonketotic-hyperglycinemia.
- Q3053945 wikiPageWikiLink Q1076421.
- Q3053945 wikiPageWikiLink Q116275.
- Q3053945 wikiPageWikiLink Q13048280.
- Q3053945 wikiPageWikiLink Q1425030.
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- Q3053945 wikiPageWikiLink Q1997.
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- Q3053945 wikiPageWikiLink Q54196.
- Q3053945 wikiPageWikiLink Q620730.
- Q3053945 wikiPageWikiLink Q6279182.
- Q3053945 wikiPageWikiLink Q6531938.
- Q3053945 wikiPageWikiLink Q6812688.
- Q3053945 wikiPageWikiLink Q6902466.
- Q3053945 wikiPageWikiLink Q7187.
- Q3053945 wikiPageWikiLink Q7215445.
- Q3053945 wikiPageWikiLink Q7250337.
- Q3053945 wikiPageWikiLink Q744151.
- Q3053945 wikiPageWikiLink Q754424.
- Q3053945 wikiPageWikiLink Q79749.
- Q3053945 wikiPageWikiLink Q8047.
- Q3053945 wikiPageWikiLink Q8066.
- Q3053945 wikiPageWikiLink Q884023.
- Q3053945 comment "Template:ForGlycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism. The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism. There are several forms of the disease, with varying severity of symptoms and time of onset.".
- Q3053945 label "Glycine encephalopathy".
- Q3053945 depiction Glycin_-_Glycine.svg.