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You searched for: Author/Creator Lecointe, Simon

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1. Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia. (July 2016)

2. Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model. Issue 3 (24th August 2022)

3. New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study. (6th September 2017)