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Funded Projects › FP7

NMD-CHIP · Development of targeted DNA-Chips for High Throughput Diagnosis of NeuroMuscular Disorders

FP7Status: CLOSED1 October 200830 September 2011EU funding €2,907,735

Inherited Neuromuscular Diseases (NMD) form a large group of diseases including Limb-Girdle Muscular Dystrophies (LGMD), Congenital Muscular Dystrophies (CMD), Duchenne and Becker Muscular Dystrophies (DMD/BMD), or Charcot-Marie-Tooth disease (CMT). Within a given disease group genetic and clinical heterogeneity is the hallmark. The precise diagnostic of neuromuscular diseases thus requires extensive clinical examination and targeted complementary tests. Additionally, since many of the disease causing mutations are known, molecular and genetic tests are performed to confirm and precise the diagnostic. According to presently available technologies, this is highly complex and time consuming. Thus, many patients remain devoid of genetic confirmation of their disease. More importantly, new cutting edge therapies cannot and will not be possibly envisaged in absence of a precise genetic diagnosis. New molecular diagnosis tools, enabling quick, reliable and cost-effective sequencing of numerous NMD genes are thus required. The development of such tools would allow performing the genetic diagnostic of NMDs patients. DNA chips have the potential to address this issue, in a time and cost effective way. The goal of this project is to i) design and validate a DNA Chip for sequencing genes responsible for LGMDs, CMDs, DMD/BMD, and CMTs, and ii) use the DNA Chip technology to identify new genes/mutations involved in these inherited NMD and increase the molecular diagnosis/patients ratio. This approach will be based on a gene candidate approach. NMD-Chip will thus lead to the development of a novel sensitive and reliable (98%) diagnostic tool, with time and cost effectiveness dedicated to neuromuscular disorders. In total, NMD-Chip, based on human genome knowledge and an advanced read out technology, will give patients an easy access to molecular diagnosis and will thus allow them to benefit from cutting edge therapies which are currently developed.

Consortium · 14 organisations

coordinator

INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE

FR · €400,000

participant

NEMZETI NEPEGESZSEGUGYI ES GYOGYSZERESZETI KOZPONT

HU · €192,895

participant

ACADEMISCH ZIEKENHUIS LEIDEN

NL · €250,000

participant

PARTNERCHIP SAS

FR · €300,000

participant

UNIVERSITY OF NEWCASTLE UPON TYNE

UK · €100,000

participant

PHENOSYSTEMS SA

CH · €209,851

participant

KAROLINSKA INSTITUTET

SE · €219,840

participant

ASSOCIATION INSTITUT DE MYOLOGIE

FR · €200,000

participant

UNIVERSITY COLLEGE LONDON

€275,000

participant

ASSOCIATION GENETHON

FR · €160,000

participant

JULIUS-MAXIMILIANS-UNIVERSITAT WURZBURG

DE · €150,000

participant

PHENOSYSTEMS SA

BE · €90,149

participant

UNIVERSITA DEGLI STUDI DI FERRARA

IT · €270,000

participant

TECHNISCHE UNIVERSITAET DRESDEN

DE · €90,000

Research fields

View the official record on CORDIS →

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