glycine has been researched along with Batten Turner Congenital Myopathy in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A total of four patients with myotonia congenita (MC) together with 106 normal individuals were examined." | 1.32 | Novel CLCN1 mutations in Taiwanese patients with myotonia congenita. ( Chang, LI; Chen, PR; Hsiao, KM; Jou, SB; Pan, H, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jou, SB | 1 |
| Chang, LI | 1 |
| Pan, H | 1 |
| Chen, PR | 1 |
| Hsiao, KM | 1 |
| Colding-Jørgensen, E | 1 |
| Duno, M | 1 |
| Vissing, J | 1 |
2 other studies available for glycine and Batten Turner Congenital Myopathy
| Article | Year |
|---|---|
Novel CLCN1 mutations in Taiwanese patients with myotonia congenita.
Topics: Adolescent; Adult; Aspartic Acid; Child; Chloride Channels; DNA Mutational Analysis; Female; Glycine | 2004 |
Autosomal dominant monosymptomatic myotonia permanens.
Topics: Child; DNA Mutational Analysis; Electromyography; Family Health; Glutamic Acid; Glycine; Humans; Mal | 2006 |