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The role and control of arginine levels in arginase 1 deficiency

Arginase 1 Deficiency (ARG1‐D) is a rare urea cycle disorder that results in persistent hyperargininemia and a distinct, progressive neurologic phenotype involving developmental delay, intellectual disability, and spasticity, predominantly affecting the lower limbs and leading to mobility impairment...

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Detalles Bibliográficos
Autores principales: Diaz, George A., Bechter, Mark, Cederbaum, Stephen D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091968/
https://www.ncbi.nlm.nih.gov/pubmed/36175366
http://dx.doi.org/10.1002/jimd.12564

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