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Publications by Minttu Marttila

Abnormal Actin Binding of Aberrant Β-Tropomyosins Is a Molecular Cause of Muscle Weakness inTPM2-related Nemaline and Cap Myopathy

Biochemical Journal
BiochemistryCell BiologyMolecular Biology
2012English

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A Rare Structural Myopathy: Nemaline Myopathy

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Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene

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Myopathy With Abnormal Structure and Function of Muscle Mitochondria.

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An Unexpected Cause of Rhabdomyolysis and Proximal Muscle Weakness

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Anaesthetic Implications of Nemaline Rod Myopathy

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Fatal Nemaline Myopathy in Infancy

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Cap Myopathy

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Deletion of the Ste20-Like Kinase SLK in Skeletal Muscle Results in a Progressive Myopathy and Muscle Weakness

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