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Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 166-167, 2004.
Artículo en Chino | WPRIM | ID: wpr-328928
ABSTRACT
<p><b>OBJECTIVE</b>To analyze the penetrance of Leber hereditary optic neuropathy (LHON) individuals with mitochondrial DNA 11778 mutation in Shanxi.</p><p><b>METHODS</b>Allele-specific PCR was used to detect mtDNA 11778 mutation in LHON patients and their families.</p><p><b>RESULTS</b>In 17 families of the 30 families that harbored mtDNA 11778 mutation, only the probands were LHON patients. In the other 13 families, besides the probands, 72 maternal relatives carried mtDNA 11778 mutation.</p><p><b>CONCLUSION</b>The penetrance of LHON individuals with mtDNA 11778 mutation in the Shanxi area is 55.6%.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: ADN Mitocondrial / Penetrancia / Atrofia Óptica Hereditaria de Leber / Genética / Mutación Límite: Adolescente / Adulto / Niño / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2004 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: ADN Mitocondrial / Penetrancia / Atrofia Óptica Hereditaria de Leber / Genética / Mutación Límite: Adolescente / Adulto / Niño / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2004 Tipo del documento: Artículo