Jones, KJ, Kim, SS, North, KN. Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies.. Journal of Medical Genetics 35(5) : 379 1998
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Koutsopoulos, OS, Koch, C, Tosch, V, Böhm, J, North, KN, Laporte, J. Mild Functional Differences of Dynamin 2 Mutations Associated to Centronuclear Myopathy and Charcot-Marie-Tooth Peripheral Neuropathy. PLOS ONE 6(11) : e27498 2011
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Oates, EC, Rosser, AM, Hafezparast, M, Lek, M, Scoto, M, Greensmith, L, Auer-Grumbach, M, Schule, R, Herrmann, DN, Clarke, NF, et al. O.10 Mutations in a new dynein/dynactin adaptor gene cause Dominant Congenital Spinal Muscular Atrophy (DCSMA) and Hereditary Spastic Paraplegia (HSP). Neuromuscular Disorders 23(9-10) : 798 2013
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North, KN, Yang, N, Wattanasirichaigoon, D, Mills, M, Easteal, S, Beggs, AH. A common nonsense mutation results in α-actinin-3 deficiency in the general population. Nature Genetics 21(4) : 353 -354 1999
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North, KN. Neurofibromatosis 1 in childhood. Seminars in Pediatric Neurology 5(4) : 231 -242 1998
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