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Medical condition
GLYT1 encephalopathy is a rare autosmal recessive, metabolic and genetic disorder which is caused by a mutation in the SLC6A9 gene. The main features of
GLYT1_encephalopathy
Medical condition
Disorders of intracellular cobalamin metabolism Lipoate deficiency GLYT1 encephalopathy Severe liver failure can lead to hyperglycinemia, while the administration
Glycine_encephalopathy
Protein-coding gene in the species Homo sapiens
discovered in 2016 and called glycine encephalopathy with normal serum glycine (OMIM 617301), also known as GlyT1 encephalopathy. Sodium:neurotransmitter symporter
Sodium- and chloride-dependent glycine transporter 1
Sodium-_and_chloride-dependent_glycine_transporter_1
Human chromosome
Usher syndrome type II Van der Woude syndrome Variegate porphyria GLYT1 Encephalopathy G-banding ideograms of human chromosome 1 "Search results - 1[CHR]
Chromosome_1
Genetic disorder causing an exaggerated startle response
neuronal pre-synaptic glycine re-uptake transporter. In comparison to the GlyT1 transporter, found mostly in glial cells, GlyT2 helps maintain a high concentration
Hyperekplexia
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY
GLYT1 ENCEPHALOPATHY