News - EAAS - European Association for American Studies.
The region on chromosome 12 contained 15 genes, including CEP290 (or NPHP6 (MIM 610142)) (fig. 1A).Mutations in this gene have recently been associated with pleiotropic forms of Joubert syndrome.11, 12 Joubert syndrome is an autosomal recessive disorder characterized by neurological features, including psychomotor delay, hypotonia, and ataxia. A typical neuroradiological feature of Joubert.
From Deakin University, there was Prof. Jane Den Hollander - President, Prof. Gary Smith - Vice President who in charge of International Cooperation, Mr. John Molony - Vice President who in charge of International Cooperation, Mr. Carl Jones - International Director, Mr. Mike Ewing - Dean of the Faculty of Business and Law, Ms. Jane Tran - Deakin Adviser in Vietnam and Ms. Trinh Mai - Deakin.