Aspartoacylase deficiency and Canavan disease in Saudi Arabia

Author:

Ozand Pinar T.,Gascon Generoso G.,Dhalla Mohammed

Publisher

Wiley

Subject

Genetics(clinical)

Reference10 articles.

1. (1982): Spongy degeneration of the nervous system. In “Neurology of Hereditary Metabolic Diseases of Children.” New York: McGraw-Hill, pp 68-71.

2. (1980): Cultivation of skin fibroblasts. In “Genetic and Metabolic Diseases. Early Diagnosis and Prenatal Analysis.” Amsterdam, North-Holland, Elsevier, pp 793-794.

3. (1989): The clinical spectrum of Canavan disease. Personal communication.

4. N-acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophy

5. Defective biosynthesis of proteolipid protein in pelizaeus-merzbacher disease

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