Study identifies pivotal role of FIBCD1 gene in neurodevelopmental disorders

A multidisciplinary study led by Vanja Nagy (LBI-RUD/CeMM/Medical University of Vienna) and Josef Penninger (UBC/IMBA) characterized a novel gene, known as FIBCD1, to be likely causative of a new and rare neurodevelopmental disorder.

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United States ,China ,United Kingdom ,British ,Josef Penninger ,Astrid Hagelkruys ,Vanja Nagy ,Emily Henderson ,Austrian Academy Of Sciences Oe ,University Of British Columbia ,Institute Of Molecular Biotechnology ,Cemm Medical University Of Vienna ,Ludwig Boltzmann Institute Of Rare ,Cemm Research Center ,Medical University ,Ludwig Boltzmann Institute ,Undiagnosed Diseases ,Molecular Medicine ,Austrian Academy ,British Columbia ,Molecular Biotechnology ,Christopher Fell ,