Hexosaminidase a deficiency manifesting as spinal muscular atrophy of late onset
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference18 articles.
1. Juvenile GM2 gangliosidosis: Partial deficiency of bexosaminidase A
2. Adult (Chronic) GM2 Gangliosidosis
3. Clinical and genetic variations in the syndrome of adult GM2 gangliodosis resulting from hexosaminidase a deficiency
4. Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: Clinical, morphologic, and biochemical studies of nine cases
5. Juvenile spinal muscular atrophy: A new hexosaminidase deficiency phenotype
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