Associated Papers
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.
Wang X et al.
The Journal of Clinical Investigation, 2024
GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms.
Mademont-Soler I et al.
American Journal of Medical Genetics. Part A, 2021
Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans.
Alfadhel M et al.
Human Genetics, 2016
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