cblE | Homocystinuria, type cblE | Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, cblE Complementation Type | Methylcobalamin Deficiency, cblE Type
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Laboratories offering clinical testing:
Sequence analysis of the entire coding regionAnalyteDeletion/duplication analysisPrenatal diagnosisCarrier testing
Baylor College of Medicine
Medical Genetics Laboratories
Houston, TX
Christine M Eng, MD, FACMG; Lee-Jun C Wong, PhD, FACMG; Dr Sarah H Elsea, PhD, FACMG; Ankita Patel, PhD
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General University Hospital in Prague
Institute of Inherited Metabolic Disorders
Praha, Czech Republic
Professor Viktor Kozich, PhD, MD
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Universidad Autonoma de Madrid
Centro de Diagnostico de Enfermedades Moleculares
Madrid, Spain
Magdalena Ugarte, PhD
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