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SPPL2C gene

Known as: IMP5, signal peptide peptidase like 2C, SPPL2C 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil
Koolen de Vries syndrome (KDVS; MIM 610443) is a genomic disorder caused by a recurrent microdeletion derived from nonallelic… 
2017
2017
Koolen de Vries syndrome: A challenge in clinical practice
2013
2013
IPF and chromosome 11p: lightning strikes twice?
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