Glycine encephalopathy

Inherited neurotransmitter diseases are a subset of rare neurometabolic disorders characterized by hereditary deficiencies in neurotransmitter metabolism or transport. Non-ketotic hyperglycinaemia (NKH), called glycine encephalopathy, is an autosomal recessive glycine metabolism disorder characteriz...

Descripción completa

Detalles Bibliográficos
Autores principales: Bhumika, S., Basalingappa, Kanthesh M., Gopenath, T. S., Basavaraju, Suman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672649/
https://www.ncbi.nlm.nih.gov/pubmed/36415754
http://dx.doi.org/10.1186/s41983-022-00567-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672649/
https://www.ncbi.nlm.nih.gov/pubmed/36415754
http://dx.doi.org/10.1186/s41983-022-00567-6

Ejemplares similares