£100.81

Humana Mitochondrial Disorders: Biochemical and Molecular Analysis

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Description

Mitochondrial diseases present significant challenges in clinical settings due to the wide variety of symptoms and the many genes involved in mitochondrial function. Because clinical manifestations are remarkably variable and heterogeneous, healthcare professionals require a structured approach to assessment and diagnosis. This volume, part of the Methods in Molecular Biology series (837), offers a systematic presentation of the protocols used to evaluate mitochondrial dysfunction. It provides cutting-edge methods of analysis designed to help laboratory and clinical experts navigate the complexities of the mitochondrial system. By offering expert guidance on how to apply these various methodologies, this book serves as a vital resource for those working in laboratory medicine and allied health professions. Whether you are conducting research or working in a clinical diagnostic environment, this text helps bridge the gap between complex genetic data and practical laboratory application.

Key Features

Provides a systematic presentation of the full range of protocols used in the assessment of mitochondrial diseases.

Offers cutting-edge methods of analysis to help manage the high variability of clinical symptoms.

Includes expert guidance on how to apply specific laboratory methodologies to evaluate dysfunction.

Addresses the complexity of the mitochondrial system and the many genes involved in its function.

Serves as a specialized resource for professionals in laboratory medicine and allied health fields.

Product Specifications

Brand
Humana
Format
paperback
Domain
Amazon UK
Release Date
23 August 2016
Listed Since
10 June 2016

Barcode

No barcode data available

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