A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder.
| Autor: | JANSSEN, R. J. R. J., WEVERS, R. A., HÄUSSLER, M., LUYTEN, J. A. F. M., STEENBERGEN-SPANJERS, G. C. H., HOFFMANN, G. F., NAGATSU, T., VAN DEN HEUVEL, L. P. W. J. |
|---|---|
| Zdroj: | Annals of Human Genetics; 09/01/2000, Vol. 64 Issue 5, p375-382, 8p |
| Databáze: | Complementary Index |
| Externí odkaz: |
|
Plný text