Francis Mastaglia

Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy

F. Mastaglia, N. Laing, J. Hallmayer, 1999, Journal of neurology, neurosurgery, and psychiatry.

A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

Liam G. Fearnley, B. Weisburd, M. Bahlo, 2023, medRxiv.

Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutation

G. Hankey, F. Mastaglia, N. Laing, 1998, Journal of neurology, neurosurgery, and psychiatry.

Investigation of muscle disease.

F. Mastaglia, N. Laing, N. G. Laing, 1996, Journal of neurology, neurosurgery, and psychiatry.

Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy

F. Mastaglia, P. Hedera, N. Laing, 2005, Journal of Neurology, Neurosurgery & Psychiatry.