A Novel Mutation of KIF11 in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR

In this study, for the first time, we describe the co-occurrence of aKIF11 mutation and 22q11.2 deletion syndrome in a patient with MCLMR.Mol Syndromol
Source: Molecular Syndromology - Category: Molecular Biology Source Type: research