BAGNEUX, France--(BUSINESS WIRE)--Regulatory News:
GENOMIC VISION (Paris:GV) (FR0011799907 – GV), a biotechnology company developing molecular and Artificial Intelligence tools to control quality and safety of genetically modified genome, is pleased to announce that the Institute of Human Genetics at the University of Duisburg in Essen (Germany), has developed a new assay to identify and characterise patients with FAME (Familial Adult Myoclonic Epilepsy) using Genomic Vision molecular combing proprietary technology and support. FAME is a rare, very slowly progressive genetically heterogeneous disorder characterised by cortical tremor and seizures. The recent publication in the prestigious journal Nature Communications “Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3” describes how molecular combing has been implemented to characterise nucleotide expansions (TTTTA/TTTCA) in a specific gene for one form of this disorder (FAME3).
Genomic Vision Molecular Combing technique proves to be a robust and accurate technique to precisely measure the variability in length and structure of these repeats and to identify for the first time micro-rearrangements occurring near or within this expansion site. Professor Christel Depienne, Ph.D. and professor at the University hospital Essen explains: “We are very pleased that molecular combing technique allowed us to characterise the expansions in FAME loci whereas methods such as next generation sequencing could not provide results with enough coverage and accuracy. We really believe that this technique has a lot of potential to characterise all forms of FAME and will lead to the development of an excellent diagnostic assay which will allow to improve the management and the quality of life of patients affected by this condition”.
The fine characterization of FAME3 patients with molecular combing has revealed an inverse correlation between the age at seizure onset and the length of the expansion, highlighting the needs to better characterize expansions in FAME patients. Aaron Bensimon, co-founder and CEO of Genomic Vision adds: “We know that Molecular Combing is the appropriate approach to assess all DNA rearrangements in genetic diseases, and in particular to size length variations of repeated regions and are confident that it will become the standard. These variations are the causes of several neurological diseases that we are currently investigating to develop new diagnostic assays. We are delighted that the Institute of Human Genetics, at the University of Duisburg-Essen uses GV’s technology to characterise the FAME condition”.
ABOUT GENOMIC VISION
Genomic Vision is a biotechnology company developing molecular and Artificial Intelligence tools to control quality and safety of genetically modified genome in particular in genome editing technologies and biomanufacturing processes.
Genomic Vision proprietary molecular tools provide robust quantitative measurements that are needed to enable high confidence characterization of DNA alteration in the genome. These tools are currently use for monitoring DNA replication in cancerous cell, for early cancer detection and the diagnosis of genetic diseases.
Based near Paris, in Bagneux, the Company has approximately 30 employees. GENOMIC VISION is a public listed company listed in compartment C of Euronext’s regulated market in Paris (Euronext: GV - ISIN: FR0011799907).
For further information, please visit www.genomicvision.com
Member of CAC® Mid & Small, CAC® All-Tradable and EnterNext© PEA-PME 150 indexes
FORWARD LOOKING STATEMENT
This press release contains implicitly or explicitly certain forward-looking statements concerning Genomic Vision and its business.
Such forward-looking statements are based on assumptions that Genomic Vision considers to be reasonable. However, there can be no assurance that such forward-looking statements will be verified, which statements are subject to numerous risks, including the risks set forth in the “Risk Factors” section of the reference document dated March 28, 2017, available on the web site of Genomic Vision (www.genomicvision.com) and to the development of economic conditions, financial markets and the markets in which Genomic Vision operates. The forward-looking statements contained in this press release are also subject to risks not yet known to Genomic Vision or not currently considered material by Genomic Vision. The occurrence of all or part of such risks could cause actual results, financial conditions, performance or achievements of Genomic Vision to be materially different from such forward-looking statements.
This press release and the information contained herein do not constitute and should not be construed as an offer or an invitation to sell or subscribe, or the solicitation of any order or invitation to purchase or subscribe for Genomic Vision shares in any country. The distribution of this press release in certain countries may be a breach of applicable laws. The persons in possession of this press release must inquire about any local restrictions and comply with these restrictions.