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Description
The ASPA gene encodes the aspartocylase, an enzyme that catalyzes the conversion of N-acetyl_L-aspartic acid (NAA) to aspartate and acetate. NAA is abundant in the brain where hydrolysis by aspartoacylase is thought to help maintain white matter. Mutations in this gene cause Canavan disease, a rare inherited disorder that affects brain development.
External Information
Click here for more information about the Canavan Syndrome genetic test.Additional information
Samples | EDTA |
---|---|
Method of testing | NGS |
Turnaround Time (TAT) | 30-40 days |
Number of Genes | 1 |
Genes / Chromosomes / SNPs | ASPA |
Related diseases | |Canavan disease |
External Information | Click here for more information about the Canavan Syndrome genetic test. |