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SETD5 gene

Known as: SETD5, SET domain containing 5, SET DOMAIN-CONTAINING PROTEIN 5 
National Institutes of Health

Papers overview

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2019
2019
A novel mutation in a common pathogenic gene (SETD5) associated with intellectual disability: A case report
Intellectual disability (ID) is a non-specific phenotype present in a genetically heterogeneous group of disorders. The genetic… 
2017
2017
De novo SETD5 loss‐of‐function variant as a cause for intellectual disability in a 10‐year old boy with an aberrant blind ending bronchus
Although rare, 3p microdeletion cases have been well described in the clinical literature. The clinical phenotype includes… 
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