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Menezes, MP, Waddell, L, Evesson, F, Cooper, S, North, KN, Clarke, NF. P1.49 The importance and challenge of diagnosing myopathies due to LMNA.
Neuromuscular Disorders
20(9-10)
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615
2010
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Quinlan, KGR, Seto, JTC, Lek, M, Zheng, FX, Garton, F, Houweling, PJ, North, KN. RARE MYOPATHIES AND EXPERIMENTAL APPROACHES - POSTER PRESENTATIONS G.P.125 ACTN3 genotype influences skeletal muscle performance through alterations in calcineurin signaling.
Neuromuscular Disorders
22(9-10)
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904
2012
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Hayashi, YK, Goto, K, Noguchi, S, Matsumoto, N, Laing, N, North, K, Clark, N, Nonaka, I, Nishino, I. P.9.4 Mutation screening of a large cohort of nemaline myopathy.
Neuromuscular Disorders
23(9-10)
:
784
2013
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O'Grady, GL, Best, HA, Oates, EC, Kaur, S, Charlton, A, Brammah, S, Punetha, J, Kesari, A, North, KN, Ilkovski, B, et al. Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spine.
European Journal of Human Genetics
23(6)
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883 -886
2014
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GARTON, FC, NORTH, KN. The Effect of Heterozygosity for the ACTN3 Null Allele on Human Muscle Performance.
Medicine & Science in Sports & Exercise
48(3)
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509 -520
2016
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