Associated Papers
A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient.
Malerba N et al.
Frontiers in Genetics, 2018
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.
Lodder EM et al.
American Journal of Human Genetics, 2016
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