Novel <i>GJA1/Cx43</i> Variant Associated With Oculo-Dento-Digital Dysplasia Syndrome: Clinical Phenotype and Cellular Mechanisms.

Novel GJA1/Cx43 Variant Associated With Oculo-Dento-Digital Dysplasia Syndrome: Clinical Phenotype and Cellular Mechanisms.

Sargiannidou, Irene; Christophidou-Anastasiadou, Violetta; Hadjisavvas, Andreas; Tanteles, George A; Kleopa, Kleopas A.

Afiliação

Sargiannidou I; Department of Neuroscience, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Christophidou-Anastasiadou V; Clinical Genetics Center, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Hadjisavvas A; Department of Clinical Genetics, Makarios Hospital, Nicosia, Cyprus.
Tanteles GA; Department of Molecular Pathology and Electron Microscopy, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Kleopa KA; Clinical Genetics Center, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.

Front Genet ; 11: 604806, 2020.

Article em En | MEDLINE | ID: mdl-33584802