Paul de Laat

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2020
Publications (10 Years): 3

Top Topics

Atrial Fibrillation

Ejection Fraction

Mitochondrial Dna

Top Venues

Molecular genetics & genomic medicine

Journal of medical genetics

Clinical kidney journal

This page only lists publications with an associated author ORCID identifier.

Publications

Paul de Laat, Richard R Rodenburg, Nel Roeleveld, Saskia Koene, Jan A Smeitink, Mirian Ch Janssen
Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variant. Journal of medical genetics 58 (1) (2020)
Paul de Laat, Nienke van Engelen, Jack F Wetzels, Jan A M Smeitink, Mirian C H Janssen
Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up and review of the literature. Clinical kidney journal 12 (6) (2019)
Paul de Laat, Richard J Rodenburg, Jan A M Smeitink, Mirian C H Janssen
Intra-patient variability of heteroplasmy levels in urinary epithelial cells in carriers of the m.3243A>G mutation. Molecular genetics & genomic medicine 7 (2) (2018)