Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Daisy Rymen

RINT1 Bi-Allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities

American Journal of Human Genetics

English

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

English