Screen LibraryMitochondrial disorders caused by nuclear genes /
Mitochondrial cytopathies are mutations in the inherited maternal mitochondrial genome, or the nuclear DNA-mutation. Mitochondrial respiratory chain disorders (RCD) are a group of genetically and clinically heterogeneous diseases, due to the fact that protein components of the respiratory chain are...
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| Published: |
Springer,
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| Publisher Address: | New York, NY : |
| Publication Dates: | 2013. |
| Literature type: | eBook |
| Language: | English |
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| Online Access: |
http://dx.doi.org/10.1007/978-1-4614-3722-2 |
| Summary: |
Mitochondrial cytopathies are mutations in the inherited maternal mitochondrial genome, or the nuclear DNA-mutation. Mitochondrial respiratory chain disorders (RCD) are a group of genetically and clinically heterogeneous diseases, due to the fact that protein components of the respiratory chain are encoded by both mitochondrial and nuclear genomes and are essential in all cells. In addition, the biogenesis, structure and function of mitochondria, including DNA replication, transcription, and translation, all require nuclear encoded genes. Since mitochondria are present in every cell, every tissue, mitochondrial disorders usually affects multiple organs. Mitochondrial Disorders Caused by Nuclear Genes discusses the biochemical, molecular, clinical, and genetic aspects of complex dual genome mitochondrial disorders. Chapters include genes involved in mitochondrial DNA biogenesis and maintenance of mitochondrial DNA integrity, complex subunits and assembly genes, and mitochondrial protein translation related diseases. |
| Carrier Form: | 1 online resource |
| Bibliography: | Includes bibliographical references and index. |
| ISBN: |
9781461437222 (electronic bk.) 1461437229 (electronic bk.) |
| Index Number: | RB147 |
| CLC: | R363.1 |
| Contents: |
Overview -- The Clinical Spectrum of Nuclear DNA-Related Mitochondrial Disorders / Biochemical and Molecular Methods for the Study of Mitochondrial Disorders / Genes Involved in Mitochondrial DNA Biogenesis and Maintenance of Mitochondrial DNA Integrity -- Mitochondrial Disorders Associated with the Mitochondrial DNA Polymerase g: A Focus on Intersubunit Interactions / Alpers-Huttenlocher Syndrome, Polymerase Gamma 1, and Mitochondrial Disease / Deoxyguanosine Kinase / MPV17-Associated Hepatocerebral Mitochondrial DNA Depletion Syndrome / Mitochondrial DNA Depletion due to Mutations in the TK2 Gene / Mitochondrial DNA Multiple Deletion Syndromes, Autosomal Dominant and Recessive (POLG, POLG2, TWINKLE and ANT1) / Defects in Mitochondrial Dynamics and Mitochondrial DNA Instability / Depletion of mtDNA with MMA: SUCLA2 and SUCLG1 / RRM2B-Related Mitochondrial Disease / Complex Subunits and Assembly Genes -- Complex Subunits and Assembly Genes: Complex I / Mitochondrial Respiratory Chain Complex II / Mitochondrial Complex III Deficiency of Nuclear Origin: / Mitochondrial Cytochrome c Oxidase Assembly in Health and Human Diseases / Mitochondrial Protein Translation Related Diseases -- Mitochondrial Aminoacyl-tRNA Synthetases / Mitochondrial Protein Translation-Related Disease: Mitochondrial Ribosomal Proteins and Translation Factors / Disorders of Mitochondrial RNA Modification / Others -- Pyruvate Dehydrogenase Complex Deficiencies / Nuclear Genes Causing Mitochondrial Cardiomyopathy / Mitochondrial Diseases Caused by Mutations in Inner Membrane Chaperone Proteins / |