Title : Myelin lipid abnormalities in the aspartoacylase-deficient tremor rat.

Pub. Date : 2009 Jan

PMID : 18478328






2 Functional Relationships(s)
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1 The biomedical relevance of such inquiries is highlighted by the myelin-associated pathology of Canavan disease, an inherited childhood disorder resulting from mutation of aspartoacylase (ASPA), the NAA-hydrolyzing enzyme. N-acetylaspartate aspartoacylase Rattus norvegicus
2 The biomedical relevance of such inquiries is highlighted by the myelin-associated pathology of Canavan disease, an inherited childhood disorder resulting from mutation of aspartoacylase (ASPA), the NAA-hydrolyzing enzyme. N-acetylaspartate aspartoacylase Rattus norvegicus