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Neurochemistry of Metabolic Diseases: Lysosomal Storage Diseases, Phenylketonuria & Canavan Disease
9781612096711
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Description
Metabolic disorder is caused by a gene defect, environmental factors or an unknown aetiology. Altered metabolism caused by these factors affects normal function of various organs including the brain and may lead to abnormal phenotype. Understanding agents of causing these abnormalities is useful to interpret possible targets in these diseases. This book reveals what factors contribute in lysosomal storage diseases, Phenylketonuria and Canavan disease, as they are major emerging diseases in multiethnic populations.
Product Details
73215
9781612096711
9781612096711
Data sheet
- Publication date
- 2012
- Issue number
- 1
- Cover
- hard cover
- Dimensions (mm)
- 260.00 x 180.00
- Weight (g)
- 732
- Sialidosis:: Pathophysiology & Therapeutic Approaches; Gaucher disease & therapeutic approaches; Parkinsons disease:: molecular changes & therapeutic approaches; Ataxia-telangiectasia:: Clinical symptoms & therapeutic approaches; Rett syndrome & therapeutic approaches; Krabbe Disease & therapeutical approaches; Gangliosidoses:: molecular pathology & therapeutic approaches; Enzyme replacement therapy for lysosomal storage diseases; Cell-based Gene Therapy for Lysosomal Storage Diseases; Biomarkers for lysosomal storage disorders; PKU in Turkey:: screening, diagnosis & management; Phenylketonuria & therapeutic approaches; Canavan disease:: molecular pathology, phenotype & therapeutic approaches; Index.
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