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Neurochemistry of Metabolic Diseases - Research Book

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Description

Explore the complex biological mechanisms behind metabolic disorders in this specialized scientific text. This book examines how gene defects, environmental factors, and unknown aetiology contribute to altered metabolism and abnormal phenotypes. It focuses on the impact these changes have on organ functions, particularly within the brain. Readers will gain insights into the specific factors driving lysosomal storage diseases, Phenylketonuria, and Canavan disease. As these conditions emerge as major concerns in multiethnic populations, this volume provides essential information for interpreting potential targets in clinical and laboratory research. Part of the Metabolic Diseases - Laboratory & Clinical Research Series, it serves as a resource for understanding the neurochemistry of these significant metabolic conditions.

Key Features

Covers the neurochemistry of lysosomal storage diseases, Phenylketonuria, and Canavan disease.

Explains how gene defects and environmental factors lead to altered metabolism and abnormal phenotypes.

Analyzes the effects of metabolic changes on various organs, including the brain.

Provides research-focused information on diseases emerging in multiethnic populations.

Published by Nova Science Publishers, Inc (US) as part of a specialized research series.

Product Specifications

Format
hardcover
Domain
Amazon UK
Release Date
26 March 2012
Listed Since
21 February 2011

Barcode

No barcode data available

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