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Publications by Daisy Rymen
RINT1 Bi-Allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities
American Journal of Human Genetics
Genetics
Mutations in MAGT1 Lead to a Glycosylation Disorder With a Variable Phenotype
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary