Metachromatic Leukodystrophy
Publisher
Springer New York
Reference48 articles.
1. Anlar, B., Waye, J. S., & Eng, B. (2006). Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutations. Developmental Medicine and Child Neurology, 48, 383–387. 2. Barth, M. L., Fensom, A., & Harris, A. (1994). The arylsulphatase A gene and molecular genetics of metachromatic leukodystrophy. Journal of Medical Genetics, 31, 663–666. 3. Batzios, S. P., & Zafeiriou, D. I. (2012). Developing treatment options for metachromatic leukodystrophy. Molecular Genetics and Metabolism, 105, 56–63. 4. Baumann, N., Masson, M., Carreau, V., et al. (1991). Adult forms of metachromatic leukodystrophy: Clinical and biochemical approach. Developmental Neuroscience, 13, 211–215. 5. Berger, J., Loschl, B., Bernheimer, H., et al. (1997). Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy. American Journal of Medical Genetics, 69, 335–340.
|
|