The Molecular Basis of Genetic Disorders Associated with Essential Elements Metabolism (Original Publisher)

The Molecular Basis of Genetic Disorders Associated with Essential Elements Metabolism is a first-of-its-kind, in-depth academic resource exploring the molecular, genetic, and biochemical mechanisms underlying disorders linked to essential trace elements. Published in 2024, this comprehensive volume unpacks the complex interplay between genes and elemental metabolism, offering insights into conditions such as Wilson’s disease, Menkes disease, hereditary hemochromatosis, and acrodermatitis enteropathica.

This title is ideal for molecular biologists, geneticists, medical researchers, nutrition scientists, clinicians in metabolic medicine, and postgraduate students in biomedical sciences. It also serves as a vital reference for labs studying micronutrient-related pathologies or drug development targeting metal ion transporters and regulatory pathways.

Key Features & Highlights

• A comprehensive review of genetic disorders related to essential metals such as iron, zinc, copper, manganese, and selenium
• Explains molecular pathways, including transporters, homeostatic regulators, and signaling mechanisms
• Integrates clinical phenotypes, genotype-phenotype correlations, and implications for diagnostics and therapy
• Discusses emerging therapeutic strategies and gene-editing potentials
• Includes figures, pathway diagrams, and summary tables for quick reference
• Written by domain experts, ensuring accuracy, clarity, and clinical relevance

Topics Covered

This book includes core chapters on the metabolism of essential trace elements, genetic transport disorders, metal ion homeostasis, inherited deficiencies and toxicities, and the molecular diagnosis of element-related diseases.

About the Author

The book is authored by an interdisciplinary team of internationally recognized researchers and clinicians specializing in genetics, biochemistry, and nutritional science. Their collaborative expertise ensures a robust synthesis of theory, data, and clinical translation.

Technical Specifications

• Format: PDF
• File Size: Approximately 30–50 MB
• Language: English
• Edition: 1st
• Year of Publication: 2024
• Device Compatibility: Works seamlessly on Kindle, Apple Books, Android, Windows, and most standard eReaders

Frequently Asked Questions

Q1: Is this book suitable for clinical practice or purely academic research?
A: While the content is research-intensive, the book also includes clinical insights, diagnostic markers, and treatment implications—making it useful for clinicians dealing with metabolic and genetic disorders.

Q2: Does the book include recent developments in gene therapy for element metabolism disorders?
A: Yes, the book discusses emerging approaches including gene-editing technologies and targeted molecular therapies as part of future treatment strategies.

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