René de Coo · researcher · YYNN

René de Coo

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researcher

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Works
7

mtDNA point mutations are present at various levels of heteroplasmy in human oocytes

scientific article published on 26 January 2007

Phenotypic consequences of a novelSCO2gene mutation

Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome

scientific article

Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy

scientific article

Significance of respirasomes for the assembly/stability of human respiratory chain complex I.

scientific article published on 18 June 2004

Changes in globus pallidus with (pre)term kernicterus

scientific article

COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux

scientific article published on 23 January 2013

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