Page last updated: 2024-11-08

serine and Spinal Muscular Atrophies of Childhood

serine has been researched along with Spinal Muscular Atrophies of Childhood 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.

Spinal Muscular Atrophies of Childhood: A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)

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
Kotani, T1
Sutomo, R1
Sasongko, TH1
Sadewa, AH1
Minato, T1
Fujii, E1
Endo, S1
Lee, MJ1
Ayaki, H1
Harada, Y1
Matsuo, M1
Nishio, H1

Other Studies

1 other study available for serine and Spinal Muscular Atrophies of Childhood

ArticleYear
A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins.
    Journal of neurology, 2007, Volume: 254, Issue:5

    Topics: Amino Acid Substitution; Child; Child, Preschool; Chromatography, High Pressure Liquid; Chromosomal

2007