Western blotting with diaminobenzidine detection for the diagnosis of congenital disorders of glycosylation

Author:

Artuch Rafael,Ferrer Imma,Pineda Julia,Moreno Justo,Busquets Christiane,Briones Paz,Vilaseca Maria Antonia

Publisher

Elsevier BV

Subject

General Neuroscience

Reference15 articles.

1. Optimised protein diagnosis in the autosomal recessive limb-girdle muscular dystrophies;Anderson;Neuromusc. Disord.,1996

2. Congenital disorders of glycosylation in 31 Spanish patients;Briones;J. Inherit. Metab. Dis.,2001

3. Personal experience with the application of CDT assays to the detection of congenital disorders of glycosylation;Colomé;Clin. Chem. Lab. Med.,2000

4. A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases;De Lonlay;J. Med. Genet.,2001

5. Congenital disorders of glycosylation: a review;Grünewald;Pediatr. Res.,2002

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