Constantinou, PanayiotisLochhead, PaulD'Allesandro, MariellaSamant, ShalakaDeciphering Developmental Disorders StudyDean, JohnHauptfleisch, Catherine2016-12-072016-12-072015Constantinou, P, Lochhead, P, D'Allesandro, M, Samant, S, Deciphering Developmental Disorders Study, Dean, J & Hauptfleisch, C 2015, 'A New, Atypical Case of Cobalamin F Disorder Diagnosed by Whole Exome Sequencing', Molecular Syndromology, vol. 6, pp. 254-258 . https://doi.org/10.1159/000441134http://hdl.handle.net/2164/7833The Deciphering Developmental Disorders Study presents independent research commissioned by the Health Innovation Challenge Fund (HICF-1009-003), a parallel funding partnership between the Wellcome Trust and the Department of Health, and the Wellcome Trust Sanger Institute (WT098051). The views expressed in this publication are those of the author(s) and not necessarily those of the Wellcome Trust or the Department of Health. The research team acknowledges the support of the National Institute for Health Research, through the Comprehensive Clinical Research Network.5444280engCobalamin F disorderLMBRD1 mutationQH426 GeneticsR MedicineGeneral Biochemistry,Genetics and Molecular BiologyGeneral MedicineWellcome TrustHealth Innovation Challenge Fund (HICF-1009-003)QH426RJournal article10.1159/0004411346