Associated Papers
Further evidence for distinct traits associated with RBM10 missense variants.
Poulton C et al.
Clinical Genetics, 2022
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features.
Kumps C et al.
Clinical Genetics, 2021
A novel missense variant in RBM10 can cause a mild form of TARP syndrome with developmental delay and dysmorphic features.
Imagawa E et al.
Clinical Genetics, 2020
First reported adult patient with TARP syndrome: A case report.
Højland AT et al.
American Journal of Medical Genetics. Part A, 2018
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