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A new neurodevelopmental disorder linked to heterozygous variants in UNC79.

May 22, 2023

ABOUT THE CONTRIBUTORS

  • Allan Bayat

    Department of Regional Health Research, University of Southern Denmark, Odense, Denmark; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark; Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark. Electronic address: abaya@filadelfia.dk.

    Zhenjiang Liu

    Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA; National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University, Changchun, 130012, China.

    Sheng Luo

    Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, the Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.

    Christina D Fenger

    Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark; Amplexa Genetics A/S, Odense. Denmark.

    Anne F Hojte

    Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark.

    Bertrand Isidor

    Department of Genetics, CHU Nantes, Nantes, France; University of Nantes, CNRS, INSERM, l’institut du thorax, Nantes, France.

    Benjamin Cogne

    Department of Genetics, CHU Nantes, Nantes, France; University of Nantes, CNRS, INSERM, l’institut du thorax, Nantes, France.

    Austin Larson

    University of Colorado School of Medicine and Children’s Hospital Colorado, Aurora, CO, United States.

    Caterina Zanus

    Institute for Maternal and Child Health, IRCCS “Burlo Garofalo”, Trieste, Italy.

    Faletra Flavio

    Institute for Maternal and Child Health, IRCCS “Burlo Garofalo”, Trieste, Italy.

    Boris Keren

    Department of Neurology, Epileptology Unit, Reference Center for Rare Epilepsies, Sorbonne University, La Pitié-Salpêtrière Hospital, AP-HP, Paris, France.

    Luciana Musante

    Institute for Maternal and Child Health, IRCCS “Burlo Garofalo”, Trieste, Italy.

    Isabelle Gourfinkel-An

    Department of Neurology, Epileptology Unit, Reference Center for Rare Epilepsies, Sorbonne University, La Pitié-Salpêtrière Hospital, AP-HP, Paris, France.

    Charles Perrine

    Department of Medical Genetics, Pitié-Salpêtrière Hospital, AP-HP, University of Sorbonne, Paris, France.

    Caroline Demily

    GénoPsy, Reference Center for Diagnosis and Management of Genetic Psychiatric Disorders, Vinatier Hospital Center and EDR-Psy Team (National Center for Scientific Research and Lyon 1 Claude Bernard University), Lyon, France; iMIND Excellence Center for Autism and Neurodevelopmental Disorders, Lyon, France.

    Gaeton Lesca

    Department of Medical Genetics, University Hospital of Lyon, Lyon, France.

    Weiping Liao

    Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, the Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China. Electronic address: wpliao@163.net.

    Dejian Ren

    Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.

REFERENCES & ADDITIONAL READING

PubMed

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