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Journal of Neuromuscular Diseases|November 19, 2016
A Large Deletion Affecting TPM3, Causing Severe Nemaline MyopathyK Kiiski, V-L Lehtokari, A Y Manzur, et al.
Neuromuscular Disorders : NMD|September 27, 2012
Targeted array comparative genomic hybridization--a new diagnostic tool for the detection of large copy number variations in nemaline myopathy-causing genesK Kiiski, L Laari, V-L Lehtokari, et al.
European Journal of Neurology|March 3, 2018
Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodiesY Nilipour, S Nafissi, A E Tjust, et al.
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