Page last updated: 2024-11-08

alanine and Classic Galactosemia

alanine has been researched along with Classic Galactosemia in 1 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Research Excerpts

ExcerptRelevanceReference
"Galactokinase deficiency is an inborn error of galactose metabolism whose major clinical manifestation is the development of cataracts during the first months of life."1.31Novel mutations in the GALK1 gene in patients with galactokinase deficiency. ( Angelicheva, D; Hunter, M; Kalaydjieva, L; Levy, HL; Pueschel, SM, 2001)

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
Hunter, M1
Angelicheva, D1
Levy, HL1
Pueschel, SM1
Kalaydjieva, L1

Other Studies

1 other study available for alanine and Classic Galactosemia

ArticleYear
Novel mutations in the GALK1 gene in patients with galactokinase deficiency.
    Human mutation, 2001, Volume: 17, Issue:1

    Topics: Adolescent; Adult; Alanine; Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Child,

2001