Reversibility of motor dysfunction in the rat model of NGLY1 deficiency

N-glycanase 1 (NGLY1) deficiency is a rare inherited disorder characterized by developmental delay, hypolacrima or alacrima, seizure, intellectual disability, motor deficits, and other neurological symptoms. The underlying mechanisms of the NGLY1 phenotype are poorly understood, and no effective the...

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Detalles Bibliográficos
Autores principales: Asahina, Makoto, Fujinawa, Reiko, Hirayama, Hiroto, Tozawa, Ryuichi, Kajii, Yasushi, Suzuki, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201687/
https://www.ncbi.nlm.nih.gov/pubmed/34120625
http://dx.doi.org/10.1186/s13041-021-00806-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201687/
https://www.ncbi.nlm.nih.gov/pubmed/34120625
http://dx.doi.org/10.1186/s13041-021-00806-6

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