Mutations in GPAA1 , Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
Thi Tuyet Mai Nguyen(Centre Hospitalier Universitaire Sainte-Justine), Philippe M. Campeau(Centre Hospitalier Universitaire Sainte-Justine), Laura Fairbrother(Vanderbilt University Medical Center), Christopher J. Carroll(St George's, University of London), Pirjo Isohanni(University of Helsinki), Tyler Reimschisel(Vanderbilt University), Joseph G. Gleeson(Children’s Institute), Maha S. Zaki(National Water Research Center), Elizabeth Berry‐Kravis(Rush University Medical Center), Norbert Fonya Ajeawung(Centre Hospitalier Universitaire Sainte-Justine), Μ. Scott Perry(Centre Hospitalier Universitaire Sainte-Justine), Alexandra Bateman(National Oceanic and Atmospheric Administration), David Parry(AstraZeneca (United Kingdom)), Clare V. Logan(University of Leeds), Fan Xia(Baylor Genetics), Colin A. Johnson(University of Leeds), Eamonn Sheridan(St James's University Hospital), Jill A. Rosenfeld(Baylor College of Medicine), Erika Ignatius(University of Helsinki), Sophie Ehresmann(Centre Hospitalier Universitaire Sainte-Justine), Tuula Lönnqvist(University of Helsinki), Guoliang Chai(Capital Medical University), Michael Parker(University of Oxford), Taroh Kinoshita(The University of Osaka), Justine Rousseau(Centre Hospitalier Universitaire Sainte-Justine), Christine P. Diggle(St James's University Hospital), Jessica Tardif(Centre Hospitalier Universitaire Sainte-Justine), Louise Hattingh(Bradford Royal Infirmary), Françoise Le Deist(Centre National de la Recherche Scientifique), Yoshiko Murakami(Hidaka Hospital), Christopher Bennett, Anik St‐Denis(Centre Hospitalier Universitaire Sainte-Justine)
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