threonine and Glycogen Storage Disease Type II

threonine has been researched along with Glycogen Storage Disease Type II in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hirschhorn, R; Martiniuk, F; Tzall, S; Zhong, N	1

Other Studies

1 other study(ies) available for threonine and Glycogen Storage Disease Type II

Article	Year
Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele. American journal of human genetics, 1991, Volume: 49, Issue:3 Topics: alpha-Glucosidases; Base Sequence; Blotting, Southern; Cell Line; Cloning, Molecular; Endonucleases; Female; Glycogen Storage Disease Type II; Humans; Methionine; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Protein Conformation; Threonine; White People	1991

Article

Year

Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele.

American journal of human genetics, 1991, Volume: 49, Issue:3

Topics: alpha-Glucosidases; Base Sequence; Blotting, Southern; Cell Line; Cloning, Molecular; Endonucleases; Female; Glycogen Storage Disease Type II; Humans; Methionine; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Protein Conformation; Threonine; White People

1991