Since the human mitochondrial genome was characterised and sequenced in 1981(l), it has been viewed as the likely site of genetic diseases showing a maternal inheritance pattern and associated with defects of the respiratory chain, such as the mitochondrial myopathies ( MMS)?(~). The properties that
β¦ LIBER β¦
Mitochondrial DNA and Genetic Disease
β Scribed by JOANNA POULTON
- Book ID
- 115266277
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 626 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0012-1622
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Mitochondrial DNA and genetic disease
β
Jo Poulton
π
Article
π
1992
π
John Wiley and Sons
π
English
β 770 KB
Ophthalmoplegia due to mitochondrial DNA
β
Andrew M. Schaefer; Emma L. Blakely; Philip G. Griffiths; Douglass M. Turnbull;
π
Article
π
2005
π
John Wiley and Sons
π
English
β 113 KB
## Abstract We describe a patient with chronic progressive external ophthalmoplegia (CPEO) who underwent muscle biopsy for suspected mitochondrial disease. In spite of normal histocytochemical cytochrome __c__ oxidase (COX) activity and respiratory chain enzyme measurements in muscle, subsequent mo
Mitochondrial DNA polymorphisms and hapl
β
Helen Latsoudis; Cleanthe Spanaki; Grigoris Chlouverakis; Andreas Plaitakis
π
Article
π
2008
π
Nature Publishing Group
π
English
β 218 KB
Mitochondrial DNA and disease
β
Patrick F Chinnery; Douglass M Turnbull
π
Article
π
1998
π
Elsevier Science
π
English
β 53 KB
Mitochondrial genetics and disease
β
Eric A. Schon
π
Article
π
2000
π
Elsevier Science
π
English
β 247 KB
Mitochondrial diseases: genetics
β
Eric A. Schon; Mark H. Grossman
π
Article
π
1998
π
IOS Press
π
English
β 159 KB