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Aceruloplasminemia

Om Aceruloplasminemia

"Aceruloplasminemia: Understanding the Rare Genetic Disorder" is an informative and insightful book that delves into the complex world of a rare genetic disorder that affects iron metabolism and can lead to neurodegeneration. This comprehensive guide provides an in-depth understanding of the clinical manifestations, biochemical features, genetic variants, and advanced imaging techniques used for diagnosis. The book also explores the mechanisms of iron-induced neurotoxicity and the role of ceruloplasmin in iron metabolism. This book is an invaluable resource for researchers, clinicians, and patients alike, providing a thorough understanding of the disease and its impact on the global population. With its concise yet comprehensive coverage of the subject matter, this book is sure to be a must-read for anyone seeking to deepen their knowledge of this rare genetic disorder.

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  • Språk:
  • Engelska
  • ISBN:
  • 9789357333450
  • Format:
  • Häftad
  • Sidor:
  • 176
  • Utgiven:
  • 6. juni 2023
  • Mått:
  • 152x10x229 mm.
  • Vikt:
  • 265 g.
  Fri leverans
Leveranstid: 2-4 veckor
Förväntad leverans: 17. december 2024

Beskrivning av Aceruloplasminemia

"Aceruloplasminemia: Understanding the Rare Genetic Disorder" is an informative and insightful book that delves into the complex world of a rare genetic disorder that affects iron metabolism and can lead to neurodegeneration. This comprehensive guide provides an in-depth understanding of the clinical manifestations, biochemical features, genetic variants, and advanced imaging techniques used for diagnosis. The book also explores the mechanisms of iron-induced neurotoxicity and the role of ceruloplasmin in iron metabolism. This book is an invaluable resource for researchers, clinicians, and patients alike, providing a thorough understanding of the disease and its impact on the global population. With its concise yet comprehensive coverage of the subject matter, this book is sure to be a must-read for anyone seeking to deepen their knowledge of this rare genetic disorder.

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