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Leber’s hereditary optic neuropathy (LHON) in an Apulian cohort of subjects
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited disorder that causes severe loss of sight in young adults, and is typically associated to mitochondrial DNA (mtDNA) mutations. Heteroplasmy of primary LHON mutations, presence of ‘ancillary’ mtDNA mutations, and mtDNA copy number a...
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| Publicado no: | Acta Myol |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pacini Editore srl
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5953227/ https://ncbi.nlm.nih.gov/pubmed/29774306 |
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