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E. Nuutinen
E. Nuutinen
University of Helsinki
Genetics
Biology
Beta-Tropomyosin
Cap myopathy
Nemaline myopathy
5
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G.P.7.09 Functional studies of aberrant beta-tropomyosin causing nemaline myopathy and cap myopathy
2009
Neuromuscular Disorders
M. Marttila
E. Nuutinen
Mubashir Hanif
Tuula A. Nyman
Kati Donner
Katarina Pelin
Mikaela Grönholm
Carina Wallgren-Pettersson
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G.P.13.02 Functional study of mutated beta-tropomyosin causing nemaline myopathy, cap myopathy and distal arthrogryposis
2008
Neuromuscular Disorders
M. Marttila
E. Nuutinen
D. Brudzewsky
S. Ollila
Kati Donner
Katarina Pelin
Carina Wallgren-Pettersson
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G.P.9.03 Characterization of the nebulin promoter and detection of brain-specific transcripts
2008
Neuromuscular Disorders
Susanna Ranta
Vilma-Lotta Lehtokari
E. Nuutinen
D. Brudzewsky
Carina Wallgren-Pettersson
Katarina Pelin
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C.P.1.12 One causative gene, TPM2, and two congenital myopathies. A functional study
2007
Neuromuscular Disorders
D. Brudzewsky
M. Marttila
E. Nuutinen
S. Ollila
Kati Donner
Katarina Pelin
Carina Wallgren-Pettersson
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G.P.8 01 Development of the multiplex ligation-dependent probe amplification (MLPA) method for the detection of large deletions in the nebulin gene
2006
Neuromuscular Disorders
Vilma-Lotta Lehtokari
Katarina Pelin
E. Nuutinen
Carina Wallgren-Pettersson
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