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Publications by Carina Wallgren-Pettersson
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
American Journal of Human Genetics
Genetics
Abnormal Actin Binding of Aberrant Β-Tropomyosins Is a Molecular Cause of Muscle Weakness inTPM2-related Nemaline and Cap Myopathy
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
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