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Oxford University Hospitals NHS Foundation Trust

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Neuromuscular and Neurodevelopmental Services

The laboratory provides the following services (R codes relate to the NHS England National Genomic Test Directory):

R80    Congenital myasthenic syndrome

Testing for previously identified familial variants, as clinically appropriate, is available.

For non NHS test requests, individual gene testing is available on request, as appropriate.

For Ataxia and Joubert syndrome and related disorders:
Refer to our list of current disease services for information on all molecular genetic services provided by the laboratory.

Also, as a Genomic Medicine Service provider, we are in the process of implementing the National Test Directory

Last updated: 12-Nov-2019 by Claire Scott

DEPARTMENTS AND SERVICES