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Paper Details

A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia.
Cold Spring Harb Mol Case Stud
15
2016
Author NameAffiliation
Szabolcs SzelingerCenter for Rare Childhood Disorders and Neurogenomics Division Translational Genomics Research Institute
David W CraigCenter for Rare Childhood Disorders and Neurogenomics Division Translational Genomics Research Institute
Matthew J HuentelmanCenter for Rare Childhood Disorders and Neurogenomics Division Translational Genomics Research Institute
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Datasets

Release 1.2