Found: 7
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Enfermedades genéticas del ADN mitocondrial humano.
- Published in:
- Salud Pública de México, 2001, v. 43, n. 2, p. 151, doi. 10.1590/S0036-36342001000200010
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- Article
Molecular Genetics of a Patient with Mohr–Tranebjaerg Syndrome due to a New Mutation in the DDP1 Gene.
- Published in:
- NeuroMolecular Medicine, 2007, v. 9, n. 4, p. 285, doi. 10.1007/s12017-007-8000-3
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- Article
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion.
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- Annals of Neurology, 2006, v. 59, n. 2, p. 394
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- Article
Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene.
- Published in:
- Annals of Neurology, 2003, v. 54, n. 4, p. 527
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- Article
De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA.
- Published in:
- Pediatric Nephrology, 2004, v. 19, n. 7, p. 790, doi. 10.1007/s00467-004-1473-5
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- Article
Expanding the clinical phenotypes of MT-ATP6 mutations.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 23, p. 6191
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- Article
Free radicals-mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA
- Published in:
- FEBS Letters, 2005, v. 579, n. 30, p. 6909, doi. 10.1016/j.febslet.2005.11.034
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- Article