Page last updated: 2024-11-08

serine and Autosomal Dominant Striatonigral Degeneration

serine has been researched along with Autosomal Dominant Striatonigral Degeneration in 1 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Research

Studies (1)

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

Authors

AuthorsStudies
Casseron, W1
Azulay, JP1
Guedj, E1
Gastaut, JL1
Pouget, J1

Other Studies

1 other study available for serine and Autosomal Dominant Striatonigral Degeneration

ArticleYear
Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability.
    Journal of neurology, 2005, Volume: 252, Issue:12

    Topics: Adult; Basal Ganglia; Cerebral Cortex; DNA Mutational Analysis; Family Health; Humans; Machado-Josep

2005