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Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency
by
Morán, María
,
Marín-Buera, Lorena
,
Gil-Borlado, M. Carmen
,
Rivera, Henry
,
Blázquez, Alberto
,
Seneca, Sara
,
Vázquez-López, María
,
Arenas, Joaquín
,
Martín, Miguel A
,
Ugalde, Cristina
Published in
Human mutation
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Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency
by
Gil-Borlado, M Carmen
,
González-Hoyuela, Maritza
,
Blázquez, Alberto
,
García-Silva, M Teresa
,
Gabaldón, Toni
,
Manzanares, Javier
,
Vara, Julia
,
Martín, Miguel A
,
Seneca, Sara
,
Arenas, Joaquín
,
Ugalde, Cristina
Published in
Mitochondrion
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Human Mutation
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Mitochondrion
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Atpases Associated With Diverse Cellular Activities
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Electron Transport Complex Iii - Deficiency
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Electron Transport Complex Iii - Genetics
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Female
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Genetics & Heredity
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Humans
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Infant, Newborn
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Life Sciences & Biomedicine
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Male
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Mitochondria
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Respiratory Chain Complex Iii Deficiency
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Science & Technology
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5' Untranslated Regions - Genetics
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Antioxidants - Metabolism
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Apoptosis
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Assembly Impairment
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Base Sequence
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Bcs1L
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Bcs1L Mutations
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Blotting, Western
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Science Citation Index Expanded (Web Of Science)
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Wiley Online Library Backfiles Complete
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