Article
Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations.
European journal of medical genetics - 1 Jun 2022
Cingöz Sultan, Soydemir Didem, Öner Tülay Öncü, Karaca Ezgi, Özden Burcu, Kurul Semra Hız, Bayram Erhan, Coe Bradley P, Nickerson Deborah A, Eichler Evan E
Abstract excerpt
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies (IDDFSDA) is an autosomal recessive multisystem disorder caused by compound heterozygous or homozygous variants in the gene OTUD6B. Herein, we describe novel pathogenic compound heterozygous variants in OTUD6B identified via whole-exome sequencing in an index case exhibited the severe IDDFSDA phenotype. The potential...
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