glycine has been researched along with Dental Enamel Hypoplasia in 2 studies
Dental Enamel Hypoplasia: An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Junctional epidermolysis bullosa is a heterogeneous autosomal recessively inherited blistering skin disorder associated with fragility at the dermal-epidermal junction." | 1.29 | Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition. ( Christiano, AM; Dunnill, MG; Eady, RA; Gatalica, B; Li, K; McGrath, JA; McMillan, JR; Uitto, J, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| McGrath, JA | 1 |
| Gatalica, B | 1 |
| Li, K | 1 |
| Dunnill, MG | 1 |
| McMillan, JR | 1 |
| Christiano, AM | 1 |
| Eady, RA | 1 |
| Uitto, J | 1 |
| Ionasescu, V | 1 |
| Stegink, L | 1 |
| Mueller, S | 1 |
| Weinstein, M | 1 |
2 other studies available for glycine and Dental Enamel Hypoplasia
| Article | Year |
|---|---|
Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.
Topics: Base Sequence; Collagen; Dental Enamel; Dental Enamel Hypoplasia; Epidermolysis Bullosa, Junctional; | 1996 |
Amino acid abnormality in Sjögren-Larsson syndrome.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; G | 1973 |