Setd5 Protein

SETD5 gene variant associated with mild intellectual disability - a case report

Authors: E. Stur, L.A. Soares and I.D. Louro

The recent advent of exome sequencing has allowed for the identification of pathogenic gene variants responsible for a variety of diseases that were previously clinically diagnosed, with no underlying molecular etiology. Among these conditions, intellectual disability is a prevalent heterogeneous condition, presenting itself i.. Read More»

Genet. Mol. Res. 16(2):

gmr16029615

DOI:

10.4238/gmr16029615