Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation APOB c.1468C\textgreaterT - Inserm - Institut national de la santé et de la recherche médicale Accéder directement au contenu
Article Dans Une Revue Clinical Chemistry and Laboratory Medicine Année : 2023

Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation APOB c.1468C\textgreaterT

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inserm-04431639 , version 1 (01-02-2024)

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Z. Henry, A. Janin, S. Nony, O. Marmontel, B. Cariou, et al.. Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation APOB c.1468C\textgreaterT. Clinical Chemistry and Laboratory Medicine, 2023, 61 (12), pp.e259-e262. ⟨10.1515/cclm-2023-0330⟩. ⟨inserm-04431639⟩
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