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Bönnemann, CG, Wong, J, Jones, KJ, Lidov, HGW, Feener, CA, Shapiro, F, Darras, BT, Kunkel, LM, North, KN.
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile..
Neuromuscul Disord
12(3)
:
273 -280
2002
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He, Y, Jones, KJ, Vignier, N, Morgan, G, Chevallay, M, Barois, A, Estournet-Mathiaud, B, Hori, H, Mizuta, T, Tomé, FM, et al.
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study..
Neurology
57(7)
:
1319 -1322
2001
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Jones, KJ, Morgan, G, Johnston, H, Tobias, V, Ouvrier, RA, Wilkinson, I, North, KN.
The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review..
J Med Genet
38(10)
:
649 -657
2001
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Ryan, MM, Schnell, C, Strickland, CD, Shield, LK, Morgan, G, Iannaccone, ST, Laing, NG, Beggs, AH, North, KN.
Nemaline myopathy: a clinical study of 143 cases..
Ann Neurol
50(3)
:
312 -320
2001
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Mills, M, Yang, N, Weinberger, R, Vander Woude, DL, Beggs, AH, Easteal, S, North, K.
Differential expression of the actin-binding proteins, alpha-actinin-2 and -3, in different species: implications for the evolution of functional redundancy..
Hum Mol Genet
10(13)
:
1335 -1346
2001
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