Sialidosis Type 1

Author:

SWALLOW DALLAS M.,EVANS LORRAINE,STEWART G.,THOMAS P. K.,ABRAMS J. D.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. Spectrofluorimetric determination of acid phosphatase activity;Campbell;Clin chim. Acta,1961

2. Electrophoretic abiiormalities of lysosoinal enzymes in mucollpidosis fibroblast lines;Champion;Am. J. hum. Genet.,1977

3. Sialidosis (Mucolipidosis I);Durand;Helv. Paediatr. Acta,1977

4. The drficicncy of a lysosomal acid hydrolase in two clones derived from the human lymplioblastoid line F137 after mutagen treatment;Gardiner;Ann. Hum. Genet., Land.,1977

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1. Type I sialidosis, a normosomatic lysosomal disease, in the differential diagnosis of late-onset ataxia and myoclonus: An overview;Molecular Genetics and Metabolism;2020-02

2. Sialidosis ☆;Reference Module in Neuroscience and Biobehavioral Psychology;2017

3. Sialidosis;Encyclopedia of Movement Disorders;2010

4. Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case;Clinical Genetics;2008-04-23

5. Inherited Epilepsies;Neurological Disease and Therapy;2005-11

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