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Bert Smeets
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TBD
researcher ORCID ID = 0000-0003-1620-908X
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Works
4
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
article
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
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Website
cris.maastrichtuniversity.nl
Instance of
Human
Occupation
university teacher
Researcher
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