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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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Biallelicframeshift mutation in RIN2 in a patient with intellectual disability and cataract, without RIN2 syndrome
Claudia J M van Amen-Hellebrekers1, Sandra Jansen1, Alexander P A Stegmann2
1Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
American Journal of Medical Genetics. Part A
|October 20, 2017
Abstract
No abstract available in PubMed .
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