Page last updated: 2024-11-08

serine and Acid Alpha-Glucosidase Deficiency

serine has been researched along with Acid Alpha-Glucosidase Deficiency 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 Excerpts

ExcerptRelevanceReference
"Glycogen storage disease type II (GSD II) is an autosomal recessive disorder resulting from a deficiency of acid alpha-glucosidase (GAA, or acid maltase)."1.33Two new missense mutations of GAA in late onset glycogen storage disease type II. ( Kim, CM; Kim, DS; Lee, CH; Park, KH; Park, YE, 2006)

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
Park, YE1
Park, KH1
Lee, CH1
Kim, CM1
Kim, DS1

Other Studies

1 other study available for serine and Acid Alpha-Glucosidase Deficiency

ArticleYear
Two new missense mutations of GAA in late onset glycogen storage disease type II.
    Journal of the neurological sciences, 2006, Dec-21, Volume: 251, Issue:1-2

    Topics: Adult; alpha-Glucosidases; Child; DNA Mutational Analysis; Family Health; Female; Glycogen Storage D

2006