Identification and expression of eight novel mutations among non-Jewish patients with Canavan disease

Canavan disease is inherited as an autosomal recessive trait that is caused by the deficiency of aspartoacylase (ASPA). The majority of patients with Canavan disease are from an Ashkenazi Jewish background. Mutations in ASPA that lead to loss of enzymatic activity have been identified, and E285A and...

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Veröffentlicht in:American journal of human genetics 1996-07, Vol.59 (1), p.95-102
Hauptverfasser: KAUL, R, GAO, G. P, MATALON, R, ALOYA, M, SU, Q, JIN, M, JOHNSON, A. B, SCHUTGENS, R. B. H, CLARKE, J. T. R
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