Page last updated: 2024-11-08

serine and Orphan Diseases

serine has been researched along with Orphan Diseases 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.

Orphan Diseases: Rare diseases that have not been well studied.

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
Shaheen, R1
Rahbeeni, Z1
Alhashem, A1
Faqeih, E1
Zhao, Q1
Xiong, Y1
Almoisheer, A1
Al-Qattan, SM1
Almadani, HA1
Al-Onazi, N1
Al-Baqawi, BS1
Saleh, MA1
Alkuraya, FS1

Other Studies

1 other study available for serine and Orphan Diseases

ArticleYear
Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDH.
    American journal of human genetics, 2014, Jun-05, Volume: 94, Issue:6

    Topics: Abnormalities, Multiple; Alleles; Amino Acid Sequence; Animals; Brain Diseases; Carbohydrate Metabol

2014