21. Correspondence. Issue 5 (October 1981) Authors: Harding, A E; Thomas, P K Journal: Journal of medical genetics Issue: Volume 18:Issue 5(1981) Page Start: 399 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
22. Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease. Issue 8 (August 1994) Authors: Planté-Bordeneuve, V; Davis, M B; Maraganore, D M; Marsden, C D; Harding, A E Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 57:Issue 8(1994) Page Start: 911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
23. Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathy. Issue 5 (May 1996) Authors: Chalmers, R M; Bandmann, O; Harding, A E Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 60:Issue 5(1996) Page Start: 588 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
24. Diaphragmatic weakness in hereditary motor and sensory neuropathy. Issue 4 (April 1990) Authors: Hardie, R; Harding, A E; Hirsch, N; Gelder, C; Macrae, A D; Thomas, P K Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 53:Issue 4(1990) Page Start: 348 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
25. Distal spinal muscular atrophy with vocal cord paralysis. Issue 3 (March 1992) Authors: Pridmore, C; Baraitser, M; Brett, E M; Harding, A E Journal: Journal of medical genetics Issue: Volume 29:Issue 3(1992) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
26. Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia. Issue 6 (June 1981) Authors: Harding, A E Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 44:Issue 6(1981) Page Start: 503 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
27. Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological study. Issue 1 (July 1995) Authors: Reilly, M M; Staunton, H; Harding, A E Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 59:Issue 1(1995) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
28. Genetic aspects of autosomal dominant late onset cerebellar ataxia. Issue 6 (December 1981) Authors: Harding, A E Journal: Journal of medical genetics Issue: Volume 18:Issue 6(1981) Page Start: 436 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
29. Genetic aspects of hereditary motor and sensory neuropathy (types I and II). Issue 5 (October 1980) Authors: Harding, A E; Thomas, P K Journal: Journal of medical genetics Issue: Volume 17:Issue 5(1980) Page Start: 329 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
30. Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. Issue 12 (December 1989) Authors: Holt, I J; Miller, D H; Harding, A E Journal: Journal of medical genetics Issue: Volume 26:Issue 12(1989) Page Start: 739 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗