Page last updated: 2024-08-24

n-acetylaspartic acid and Amino Acid Transport Disorders, Inborn

n-acetylaspartic acid has been researched along with Amino Acid Transport Disorders, Inborn in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alcaide, P; Castro, P; Ferrer, I; Merinero, B; Rodriguez-Pombo, P; Ruiz Martin, Y; Ruiz-Sala, P; Ugarte, M1

Other Studies

1 other study(ies) available for n-acetylaspartic acid and Amino Acid Transport Disorders, Inborn

ArticleYear
A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene.
    Developmental medicine and child neurology, 2010, Volume: 52, Issue:2

    Topics: Amino Acid Transport Disorders, Inborn; Aspartic Acid; Brain Diseases, Metabolic, Inborn; Child, Preschool; Creatine; DNA Mutational Analysis; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Nerve Tissue Proteins; Plasma Membrane Neurotransmitter Transport Proteins; Tritium

2010