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Molecular diagnosis of Mitochondrial DNA Disease (Multigene Panel; 37 genes)
Despite our efforts to ensure that data is up to date, this activity has not been validated since 10/06/2014- Neurogenetics Unit
- Department of Molecular Neuroscience, UCL Institute of Neurology
- National Hospital for Neurology and Neurosurgery
- Queen Square, Box 102
- LONDON WC1N 3BG
- UNITED KINGDOM
- Director of laboratory : Dr Mary SWEENEY
- More information
- Phone : 44 (0)203 448 4250
- Additional Phone : 44 (0)203 448 4282
- Fax : 44 (0)203 448 8784
- Website
Last update: June 2014
Purpose(s)
Post-natal diagnosis
Technical procedure(s)
Molecular genetics
Mutation scanning/screening and sequence analysis of selected exons
NGS sequencing (except WES)
List of diseases and genes
List of diseases tested
(1)
Additional information
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.