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Year | Number of Results |
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2002 | 1 |
2009 | 1 |
2016 | 1 |
2020 | 1 |
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Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine.
Am J Hum Genet. 2016 Nov 3;99(5):1172-1180. doi: 10.1016/j.ajhg.2016.09.004. Epub 2016 Oct 20.
Am J Hum Genet. 2016.
PMID: 27773429
Free PMC article.
High glycine content in TDP-43: a potential culprit in limbic-predominant age-related TDP-43 encephalopathy.
An S, Zhang X, Shi Y, Zhang J, Wan Y, Wang Y, Zhang Y, Liu Q.
An S, et al.
J Int Med Res. 2020 Jun;48(6):300060520929853. doi: 10.1177/0300060520929853.
J Int Med Res. 2020.
PMID: 32529876
Free PMC article.
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Atypical glycine encephalopathy in an extremely low birth weight infant: description of a new mutation and clinical and electroencephalographic analysis.
Pardal-Fernández JM, Carrascosa-Romero MC, de Cabo-de la Vega C, Iniesta-López I, Gil-Pons E, Martínez-Gutiérrez A.
Pardal-Fernández JM, et al.
Epileptic Disord. 2009 Mar;11(1):48-53. doi: 10.1684/epd.2009.0249. Epub 2009 Mar 20.
Epileptic Disord. 2009.
PMID: 19299230
Free article.
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Pitfalls in the diagnosis of glycine encephalopathy (non-ketotic hyperglycinemia).
Korman SH, Gutman A.
Korman SH, et al.
Dev Med Child Neurol. 2002 Oct;44(10):712-20. doi: 10.1017/s0012162201002808.
Dev Med Child Neurol. 2002.
PMID: 12418798
Free article.
No abstract available.
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