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Journal of Clinical Investigation, ISSN 0021-9738, 08/2014, Volume 124, Issue 8, pp. 3529 - 3539
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2013, Volume 93, Issue 1, pp. 6 - 18
Journal Article
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 9/2015, Volume 130, Issue 3, pp. 389 - 406
Journal Article
Journal Article
Revue Neurologique, ISSN 0035-3787, 10/2016, Volume 172, Issue 10, pp. 614 - 619
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The condition is defined by the histopathological finding of nemaline bodies... 
Congenital myopathy | Skeletal muscle pathology | Nemaline myopathy | CORES | HYPERTROPHIC CARDIOMYOPATHY | NEBULIN GENE | MYO18B | CONGENITAL MYOPATHIES | MUTATIONS | MUSCLE ALPHA-ACTIN | CHILDHOOD | CLINICAL NEUROLOGY | Myopathies, Nemaline - genetics | Biopsy | Humans | Myopathies, Nemaline - pathology | Myopathies, Nemaline - therapy
Journal Article