Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin

Cornelis L. HarteveldHemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, the Netherlands; Correspondence[email protected]

Serge PissardLaboratory of Genetics, Assistance Publique-Hôitaux De Paris (APHP), Groupe Hospitalier Universitaire (GHU) Henri Mondor, Universite Paris Est Créteil (UPEC) and Inserm Institut Mondor De Recherche Biologique (IMRB) U955eq2, Créteil, France;

Anna M. H. KorverDepartment of Pediatrics, Groene Hart Hospital, Gouda, the Netherlands;

Jean RiouLaboratory of Genetics, Assistance Publique-Hôitaux De Paris (APHP), Groupe Hospitalier Universitaire (GHU) Henri Mondor, Créteil, France;

Eric LegacLaboratory of Biology, Centre Hospitalier Régioonale (CHR) Orleans, Orleans, France;

Gideon LansbergenClinical Chemistry, Groene Hart Hospital, Gouda, the Netherlands;

Inge L. PardijsDepartment of Pediatrics, Groene Hart Hospital, Gouda, the Netherlands; ;General Practitioner, Gouda, the Netherlands

Piero C. GiordanoHemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, the Netherlands;

Florens G. A. VersteeghDepartment of Pediatrics, Groene Hart Hospital, Gouda, the Netherlands;

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Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin

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Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin

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